Canonical Allele Identifier: CA2160591

Gene: ARMC9

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.231360884G>A , CM000664.2:g.231360884G>A	GRCh38
NC_000002.11:g.232225595G>A , CM000664.1:g.232225595G>A	GRCh37
NC_000002.10:g.231933839G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001352754.2:c.2261+1G>A MANE Select	NP_001339683.2:n.2261+1G>A
ENST00000611582.5:c.2261+1G>A MANE Select	ENSP00000484804.1:n.2261+1G>A
NM_001271466.2:c.2261+1G>A	NP_001258395.1:n.2261+1G>A
NM_001271466.3:c.2261+1G>A	NP_001258395.1:n.2261+1G>A
NM_001271466.4:c.2261+1G>A	NP_001258395.2:n.2261+1G>A
NM_001352754.1:c.2261+1G>A	NP_001339683.1:n.2261+1G>A
ENST00000611582.4:c.2261+1G>A	ENSP00000484804.1:n.2261+1G>A
ENST00000614261.4:c.2261+1G>A	ENSP00000484241.1:n.2261+1G>A
ENST00000684075.1:n.174+1G>A
XM_011511905.1:c.2145+1G>A	XP_011510207.1:n.2145+1G>A
XM_011511906.1:c.2142+1G>A	XP_011510208.1:n.2142+1G>A
XM_011511907.1:c.2046+1G>A	XP_011510209.1:n.2046+1G>A
XM_011511908.1:c.2261+1G>A	XP_011510210.1:n.2261+1G>A
XM_011511908.2:c.2261+1G>A	XP_011510210.1:n.2261+1G>A
XM_011511909.1:c.2258+1G>A	XP_011510211.1:n.2258+1G>A
XM_011511909.2:c.2258+1G>A	XP_011510211.1:n.2258+1G>A
XM_011511910.1:c.2261+1G>A	XP_011510212.1:n.2261+1G>A
XM_011511911.1:c.2261+1G>A	XP_011510213.1:n.2261+1G>A
XM_011511912.1:c.2145+1G>A	XP_011510214.1:n.2145+1G>A
XM_011511913.1:c.2145+1G>A	XP_011510215.1:n.2145+1G>A
XM_011511913.2:c.2145+1G>A	XP_011510215.1:n.2145+1G>A
XM_011511919.1:c.1071+1G>A	XP_011510221.1:n.1071+1G>A
XM_011511919.2:c.1071+1G>A	XP_011510221.1:n.1071+1G>A
XM_017005021.1:c.2261+1G>A	XP_016860510.1:n.2261+1G>A
XM_017005022.1:c.2261+1G>A	XP_016860511.1:n.2261+1G>A
XM_017005024.1:c.2162+1G>A	XP_016860513.1:n.2162+1G>A
XM_017005025.1:c.2145+1G>A	XP_016860514.1:n.2145+1G>A