Canonical Allele Identifier: CA16384394
Gene: ACBD5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.27215406T>C , CM000672.2:g.27215406T>C GRCh38
NC_000010.10:g.27504335T>C , CM000672.1:g.27504335T>C GRCh37
NC_000010.9:g.27544341T>C NCBI36
NG_032960.2:g.31734A>G
NG_032960.3:g.38269A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000396271.8:c.936+129A>G MANE Select ENSP00000379568.3:n.936+129A>G
ENST00000676511.1:c.864+129A>G ENSP00000504333.1:n.864+129A>G
ENST00000676599.1:c.*743+129A>G ENSP00000503053.1:n.*743+129A>G
ENST00000676648.1:c.856+2574A>G ENSP00000503864.1:n.856+2574A>G
ENST00000676731.1:c.831+129A>G ENSP00000503158.1:n.831+129A>G
ENST00000676732.1:c.660+129A>G ENSP00000504029.1:n.660+129A>G
ENST00000676997.1:c.936+129A>G ENSP00000503467.1:n.936+129A>G
ENST00000677141.1:c.915+129A>G ENSP00000503831.1:n.915+129A>G
ENST00000677200.1:c.831+129A>G ENSP00000503715.1:n.831+129A>G
ENST00000677248.1:c.660+129A>G ENSP00000504367.1:n.660+129A>G
ENST00000677311.1:c.930+129A>G ENSP00000504499.1:n.930+129A>G
ENST00000677440.1:c.642+129A>G ENSP00000504580.1:n.642+129A>G
ENST00000677441.1:c.831+129A>G ENSP00000503415.1:n.831+129A>G
ENST00000677509.1:c.864+129A>G ENSP00000503264.1:n.864+129A>G
ENST00000677667.1:c.627+129A>G ENSP00000503208.1:n.627+129A>G
ENST00000677901.1:c.360+129A>G ENSP00000504374.1:n.360+129A>G
ENST00000677960.1:c.627+129A>G ENSP00000504726.1:n.627+129A>G
ENST00000678392.1:c.831+129A>G ENSP00000504666.1:n.831+129A>G
ENST00000678446.1:c.627+129A>G ENSP00000503800.1:n.627+129A>G
ENST00000679220.1:c.777+129A>G ENSP00000502986.1:n.777+129A>G
ENST00000679293.1:c.831+129A>G ENSP00000503631.1:n.831+129A>G
ENST00000375888.5:c.963+129A>G ENSP00000365049.1:n.963+129A>G
ENST00000375897.7:c.930+129A>G ENSP00000365062.4:n.930+129A>G
ENST00000375901.5:c.609+129A>G ENSP00000365066.1:n.609+129A>G
ENST00000375905.8:c.831+129A>G ENSP00000365070.4:n.831+129A>G
ENST00000396271.7:c.936+129A>G ENSP00000379568.3:n.936+129A>G
ENST00000476758.1:c.*730+129A>G ENSP00000483256.1:n.*730+129A>G
NM_001042473.3:c.831+129A>G NP_001035938.1:n.831+129A>G
NM_001271512.3:c.930+129A>G NP_001258441.1:n.930+129A>G
NM_001301251.1:c.609+129A>G NP_001288180.1:n.609+129A>G
NM_001301252.1:c.609+129A>G NP_001288181.1:n.609+129A>G
NM_001301253.1:c.609+129A>G NP_001288182.1:n.609+129A>G
NM_001301254.1:c.405+129A>G NP_001288183.1:n.405+129A>G
NM_145698.4:c.936+129A>G NP_663736.2:n.936+129A>G
XM_006717528.2:c.864+129A>G XP_006717591.2:n.864+129A>G
XM_006717530.2:c.990+129A>G XP_006717593.1:n.990+129A>G
XM_006717531.1:c.969+129A>G XP_006717594.1:n.969+129A>G
XM_006717533.2:c.660+129A>G XP_006717596.2:n.660+129A>G
XM_006717535.1:c.864+129A>G XP_006717598.1:n.864+129A>G
XM_011519759.1:c.627+129A>G XP_011518061.1:n.627+129A>G
XM_011519760.1:c.642+129A>G XP_011518062.1:n.642+129A>G
NM_001352568.1:c.990+129A>G NP_001339497.1:n.990+129A>G
NM_001352569.1:c.969+129A>G NP_001339498.1:n.969+129A>G
NM_001352570.1:c.936+129A>G NP_001339499.1:n.936+129A>G
NM_001352571.1:c.963+129A>G NP_001339500.1:n.963+129A>G
NM_001352572.1:c.957+129A>G NP_001339501.1:n.957+129A>G
NM_001352573.1:c.915+129A>G NP_001339502.1:n.915+129A>G
NM_001352574.1:c.864+129A>G NP_001339503.1:n.864+129A>G
NM_001352575.1:c.864+129A>G NP_001339504.1:n.864+129A>G
NM_001352576.1:c.864+129A>G NP_001339505.1:n.864+129A>G
NM_001352577.1:c.831+129A>G NP_001339506.1:n.831+129A>G
NM_001352578.1:c.831+129A>G NP_001339507.1:n.831+129A>G
NM_001352579.1:c.831+129A>G NP_001339508.1:n.831+129A>G
NM_001352580.1:c.777+129A>G NP_001339509.1:n.777+129A>G
NM_001352581.1:c.765+129A>G NP_001339510.1:n.765+129A>G
NM_001352582.1:c.627+129A>G NP_001339511.1:n.627+129A>G
NM_001352583.1:c.609+129A>G NP_001339512.1:n.609+129A>G
NM_001352584.1:c.609+129A>G NP_001339513.1:n.609+129A>G
NM_001352585.1:c.642+129A>G NP_001339514.1:n.642+129A>G
NM_001352586.1:c.759+129A>G NP_001339515.1:n.759+129A>G
NM_001352587.1:c.726+129A>G NP_001339516.1:n.726+129A>G
NM_001352588.1:c.732+129A>G NP_001339517.1:n.732+129A>G
XM_006717528.4:c.1161+129A>G XP_006717591.3:n.1161+129A>G
XM_017016884.2:c.1161+129A>G XP_016872373.1:n.1161+129A>G
XM_017016885.2:c.1128+129A>G XP_016872374.1:n.1128+129A>G
XM_017016886.2:c.1128+129A>G XP_016872375.1:n.1128+129A>G
XM_017016887.2:c.990+129A>G XP_016872376.1:n.990+129A>G
XM_017016888.2:c.969+129A>G XP_016872377.1:n.969+129A>G
XM_017016889.2:c.957+129A>G XP_016872378.1:n.957+129A>G
XM_017016890.2:c.957+129A>G XP_016872379.1:n.957+129A>G
XM_017016893.2:c.924+129A>G XP_016872382.1:n.924+129A>G
XM_017016894.2:c.924+129A>G XP_016872383.1:n.924+129A>G
XM_017016895.2:c.864+129A>G XP_016872384.1:n.864+129A>G
XM_017016896.1:c.831+129A>G XP_016872385.1:n.831+129A>G
XM_017016898.2:c.732+129A>G XP_016872387.1:n.732+129A>G
XM_017016900.1:c.642+129A>G XP_016872389.1:n.642+129A>G
XM_017016901.1:c.642+129A>G XP_016872390.1:n.642+129A>G
XM_017016902.1:c.642+129A>G XP_016872391.1:n.642+129A>G
XM_017016904.1:c.609+129A>G XP_016872393.1:n.609+129A>G
XM_017016905.1:c.609+129A>G XP_016872394.1:n.609+129A>G
XM_024448248.1:c.765+129A>G XP_024304016.1:n.765+129A>G
XM_024448249.1:c.753+129A>G XP_024304017.1:n.753+129A>G
NM_145698.5:c.936+129A>G MANE Select NP_663736.2:n.936+129A>G
NM_001042473.4:c.831+129A>G NP_001035938.1:n.831+129A>G
NM_001301251.2:c.609+129A>G NP_001288180.1:n.609+129A>G
NM_001301252.2:c.609+129A>G NP_001288181.1:n.609+129A>G
NM_001301253.2:c.609+129A>G NP_001288182.1:n.609+129A>G
NM_001301254.2:c.405+129A>G NP_001288183.1:n.405+129A>G
NM_001352574.2:c.864+129A>G NP_001339503.1:n.864+129A>G
NM_001352575.2:c.864+129A>G NP_001339504.1:n.864+129A>G
NM_001352577.2:c.831+129A>G NP_001339506.1:n.831+129A>G
NM_001352580.2:c.777+129A>G NP_001339509.1:n.777+129A>G
NM_001352582.2:c.627+129A>G NP_001339511.1:n.627+129A>G
NM_001352576.2:c.864+129A>G NP_001339505.1:n.864+129A>G
NM_001352578.2:c.831+129A>G NP_001339507.1:n.831+129A>G
NM_001352579.2:c.831+129A>G NP_001339508.1:n.831+129A>G
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