Canonical Allele Identifier: CA196851690
Gene: AOPEP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95018081C>A , CM000671.2:g.95018081C>A GRCh38
NC_000009.11:g.97780363C>A , CM000671.1:g.97780363C>A GRCh37
NC_000009.10:g.96820184C>A NCBI36
NG_027833.1:g.296413C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000445181.6:n.208+12465C>A
ENST00000478473.2:n.196+12465C>A
ENST00000710812.1:n.206+12465C>A
ENST00000375315.8:c.2115+12465C>A MANE Select ENSP00000364464.2:n.2115+12465C>A
ENST00000375315.7:c.2115+12465C>A ENSP00000364464.2:n.2115+12465C>A
ENST00000297979.9:c.1818+12465C>A ENSP00000297979.5:n.1818+12465C>A
ENST00000375315.6:c.2115+12465C>A ENSP00000364464.2:n.2115+12465C>A
ENST00000424143.5:c.1287+12465C>A ENSP00000402171.1:n.1287+12465C>A
ENST00000428313.5:c.1461+12465C>A ENSP00000401854.1:n.1461+12465C>A
ENST00000445181.5:c.208+12465C>A
ENST00000460573.5:n.217+12465C>A
ENST00000462125.5:n.781+12465C>A
ENST00000463372.5:n.199+12465C>A
ENST00000471978.5:n.224+12465C>A
ENST00000478473.1:c.196+12465C>A
ENST00000478603.5:n.508+12465C>A
ENST00000479161.5:n.837+12465C>A
ENST00000496567.5:n.192-1369C>A
NM_001193329.1:c.2115+12465C>A NP_001180258.1:n.2115+12465C>A
NM_032823.5:c.1818+12465C>A NP_116212.3:n.1818+12465C>A
XM_005252284.1:c.1818+12465C>A XP_005252341.1:n.1818+12465C>A
XM_006717306.1:c.2115+12465C>A XP_006717369.1:n.2115+12465C>A
XM_011519119.1:c.2115+12465C>A XP_011517421.1:n.2115+12465C>A
XM_011519120.1:c.2115+12465C>A XP_011517422.1:n.2115+12465C>A
XM_011519121.1:c.2115+12465C>A XP_011517423.1:n.2115+12465C>A
XM_011519128.1:c.1224+12465C>A XP_011517430.1:n.1224+12465C>A
XM_011519132.1:c.975+12465C>A XP_011517434.1:n.975+12465C>A
XR_929852.1:n.2398+12465C>A
XR_929853.1:n.2398+12465C>A
XR_929854.1:n.2398+12465C>A
XR_929855.1:n.2399-1369C>A
XR_929856.1:n.2399-1369C>A
XM_005252284.3:c.1818+12465C>A XP_005252341.1:n.1818+12465C>A
XM_006717306.2:c.2115+12465C>A XP_006717369.1:n.2115+12465C>A
XM_011519119.2:c.2115+12465C>A XP_011517421.1:n.2115+12465C>A
XM_011519120.3:c.2115+12465C>A XP_011517422.1:n.2115+12465C>A
XM_011519121.3:c.2115+12465C>A XP_011517423.1:n.2115+12465C>A
XM_017015229.1:c.2115+12465C>A XP_016870718.1:n.2115+12465C>A
XM_017015230.2:c.2115+12465C>A XP_016870719.1:n.2115+12465C>A
XM_017015231.2:c.1818+12465C>A XP_016870720.1:n.1818+12465C>A
XM_017015232.2:c.2116-1369C>A XP_016870721.1:n.2116-1369C>A
XM_017015233.1:c.1245+12465C>A XP_016870722.1:n.1245+12465C>A
XM_017015234.2:c.1224+12465C>A XP_016870723.1:n.1224+12465C>A
XM_017015235.2:c.1224+12465C>A XP_016870724.1:n.1224+12465C>A
XM_017015236.2:c.927+12465C>A XP_016870725.1:n.927+12465C>A
XM_017015237.2:c.927+12465C>A XP_016870726.1:n.927+12465C>A
XR_001746402.2:n.2333+12465C>A
XR_001746403.2:n.1992+12465C>A
XR_001746404.2:n.1992+12465C>A
XR_929852.2:n.2333+12465C>A
XR_929853.2:n.2333+12465C>A
XR_929854.2:n.2333+12465C>A
XR_929855.2:n.2334-1369C>A
XR_929856.3:n.2334-1369C>A
NM_001193329.3:c.2115+12465C>A MANE Select NP_001180258.1:n.2115+12465C>A
NM_001386061.1:c.825+12465C>A NP_001372990.1:n.825+12465C>A
NM_001386062.2:c.1794+12465C>A NP_001372991.1:n.1794+12465C>A
NM_001386063.2:c.1977+38654C>A NP_001372992.1:n.1977+38654C>A
NM_001386066.1:c.2115+12465C>A NP_001372995.1:n.2115+12465C>A
NM_001386067.1:c.1593+12465C>A NP_001372996.1:n.1593+12465C>A
NM_001386068.1:c.2115+12465C>A NP_001372997.1:n.2115+12465C>A
NM_001386069.1:c.1818+12465C>A NP_001372998.1:n.1818+12465C>A
NM_001386070.1:c.2115+12465C>A NP_001372999.1:n.2115+12465C>A
NM_001386074.1:c.2115+12465C>A NP_001373003.1:n.2115+12465C>A
NM_001386075.1:c.2115+12465C>A NP_001373004.1:n.2115+12465C>A
NM_001386076.1:c.2115+12465C>A NP_001373005.1:n.2115+12465C>A
NM_032823.6:c.1818+12465C>A NP_116212.3:n.1818+12465C>A
NR_169862.1:n.2196+12465C>A
NR_169863.2:n.1962+12465C>A
NR_169864.1:n.1962+12465C>A
NR_169865.1:n.2092+12465C>A
NR_169866.1:n.1795+12465C>A
NR_169867.1:n.728+12465C>A
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