Canonical Allele Identifier: CA431718687
Gene: ARMC9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.231206294G>T , CM000664.2:g.231206294G>T GRCh38
NC_000002.11:g.232071007G>T , CM000664.1:g.232071007G>T GRCh37
NC_000002.10:g.231779251G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000436339.6:c.51+5G>T ENSP00000392086.2:n.51+5G>T
ENST00000440107.6:c.51+5G>T ENSP00000387391.2:n.51+5G>T
ENST00000482392.2:n.155+5G>T
ENST00000682002.1:c.51+5G>T ENSP00000507152.1:n.51+5G>T
ENST00000682027.1:n.160+5G>T
ENST00000682030.1:c.51+5G>T ENSP00000508117.1:n.51+5G>T
ENST00000682100.1:c.51+5G>T ENSP00000507066.1:n.51+5G>T
ENST00000682233.1:n.362+5G>T
ENST00000682264.1:c.51+5G>T ENSP00000507212.1:n.51+5G>T
ENST00000682334.1:c.51+5G>T ENSP00000507763.1:n.51+5G>T
ENST00000682367.1:c.51+5G>T ENSP00000507235.1:n.51+5G>T
ENST00000682751.1:n.358+5G>T
ENST00000683040.1:c.51+5G>T ENSP00000507817.1:n.51+5G>T
ENST00000683063.1:c.51+5G>T ENSP00000507407.1:n.51+5G>T
ENST00000683107.1:n.148+5G>T
ENST00000683112.1:c.51+5G>T ENSP00000507357.1:n.51+5G>T
ENST00000683165.1:n.197+5G>T
ENST00000683271.1:c.51+5G>T ENSP00000507513.1:n.51+5G>T
ENST00000683275.1:c.51+5G>T ENSP00000506823.1:n.51+5G>T
ENST00000683321.1:c.51+5G>T ENSP00000508154.1:n.51+5G>T
ENST00000683553.1:c.51+5G>T ENSP00000506860.1:n.51+5G>T
ENST00000683575.1:c.51+5G>T ENSP00000507743.1:n.51+5G>T
ENST00000683629.1:c.51+5G>T ENSP00000507960.1:n.51+5G>T
ENST00000683702.1:c.51+5G>T ENSP00000507686.1:n.51+5G>T
ENST00000683814.1:n.362+5G>T
ENST00000683966.1:c.51+5G>T ENSP00000507325.1:n.51+5G>T
ENST00000684011.1:n.156+5G>T
ENST00000684051.1:c.51+5G>T ENSP00000507854.1:n.51+5G>T
ENST00000684368.1:c.51+5G>T ENSP00000508353.1:n.51+5G>T
ENST00000684432.1:c.51+5G>T ENSP00000508405.1:n.51+5G>T
ENST00000684565.1:c.51+5G>T ENSP00000507599.1:n.51+5G>T
ENST00000684718.1:c.51+5G>T ENSP00000507543.1:n.51+5G>T
ENST00000611582.5:c.51+5G>T MANE Select ENSP00000484804.1:n.51+5G>T
ENST00000349938.8:c.51+5G>T ENSP00000258417.5:n.51+5G>T
ENST00000440107.5:c.51+5G>T ENSP00000387391.1:n.51+5G>T
ENST00000482392.1:n.148+5G>T
ENST00000611582.4:c.51+5G>T ENSP00000484804.1:n.51+5G>T
ENST00000614261.4:c.51+5G>T ENSP00000484241.1:n.51+5G>T
NM_001271466.2:c.51+5G>T NP_001258395.1:n.51+5G>T
NM_001291656.1:c.51+5G>T NP_001278585.1:n.51+5G>T
NM_025139.5:c.51+5G>T NP_079415.3:n.51+5G>T
XM_011511905.1:c.51+5G>T XP_011510207.1:n.51+5G>T
XM_011511906.1:c.51+5G>T XP_011510208.1:n.51+5G>T
XM_011511907.1:c.51+5G>T XP_011510209.1:n.51+5G>T
XM_011511908.1:c.51+5G>T XP_011510210.1:n.51+5G>T
XM_011511909.1:c.51+5G>T XP_011510211.1:n.51+5G>T
XM_011511910.1:c.51+5G>T XP_011510212.1:n.51+5G>T
XM_011511911.1:c.51+5G>T XP_011510213.1:n.51+5G>T
XM_011511912.1:c.51+5G>T XP_011510214.1:n.51+5G>T
XM_011511913.1:c.51+5G>T XP_011510215.1:n.51+5G>T
XM_011511914.1:c.51+5G>T XP_011510216.1:n.51+5G>T
XM_011511915.1:c.51+5G>T XP_011510217.1:n.51+5G>T
XM_011511916.1:c.51+5G>T XP_011510218.1:n.51+5G>T
XM_011511917.1:c.51+5G>T XP_011510219.1:n.51+5G>T
XM_011511918.1:c.51+5G>T XP_011510220.1:n.51+5G>T
XM_011511920.1:c.51+5G>T XP_011510222.1:n.51+5G>T
XR_923031.1:n.163+5G>T
XR_923032.1:n.163+5G>T
NM_001271466.3:c.51+5G>T NP_001258395.1:n.51+5G>T
NM_001352754.1:c.51+5G>T NP_001339683.1:n.51+5G>T
NM_001352755.1:c.51+5G>T NP_001339684.1:n.51+5G>T
NM_001352756.1:c.51+5G>T NP_001339685.1:n.51+5G>T
NM_001352757.1:c.51+5G>T NP_001339686.1:n.51+5G>T
NM_001352758.1:c.51+5G>T NP_001339687.1:n.51+5G>T
NM_001352759.1:c.51+5G>T NP_001339688.1:n.51+5G>T
NR_148040.1:n.245+5G>T
XM_011511908.2:c.51+5G>T XP_011510210.1:n.51+5G>T
XM_011511909.2:c.51+5G>T XP_011510211.1:n.51+5G>T
XM_011511913.2:c.51+5G>T XP_011510215.1:n.51+5G>T
XM_011511914.2:c.51+5G>T XP_011510216.1:n.51+5G>T
XM_011511915.2:c.51+5G>T XP_011510217.1:n.51+5G>T
XM_011511916.2:c.51+5G>T XP_011510218.1:n.51+5G>T
XM_017005021.1:c.51+5G>T XP_016860510.1:n.51+5G>T
XM_017005022.1:c.51+5G>T XP_016860511.1:n.51+5G>T
XM_017005024.1:c.51+5G>T XP_016860513.1:n.51+5G>T
XM_017005025.1:c.51+5G>T XP_016860514.1:n.51+5G>T
NM_001271466.4:c.51+5G>T NP_001258395.2:n.51+5G>T
NM_001291656.2:c.51+5G>T NP_001278585.2:n.51+5G>T
NM_001352754.2:c.51+5G>T MANE Select NP_001339683.2:n.51+5G>T
NM_001352755.2:c.51+5G>T NP_001339684.2:n.51+5G>T
NM_001352756.2:c.51+5G>T NP_001339685.2:n.51+5G>T
NM_001352757.2:c.51+5G>T NP_001339686.2:n.51+5G>T
NM_001352758.2:c.51+5G>T NP_001339687.2:n.51+5G>T
NM_001352759.2:c.51+5G>T NP_001339688.2:n.51+5G>T
NM_025139.6:c.51+5G>T NP_079415.4:n.51+5G>T
NR_148040.2:n.160+5G>T
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