Canonical Allele Identifier: CA2838255086

Gene: ARMC9

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.231378758A>T , CM000664.2:g.231378758A>T	GRCh38
NC_000002.11:g.232243469A>T , CM000664.1:g.232243469A>T	GRCh37
NC_000002.10:g.231951713A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011511908.1:c.*223A>T	XP_011510210.1:n.*223A>T
XM_011511909.1:c.*223A>T	XP_011510211.1:n.*223A>T
XM_011511910.1:c.2434+8633A>T	XP_011510212.1:n.2434+8633A>T
XM_011511912.1:c.2318+8633A>T	XP_011510214.1:n.2318+8633A>T
XM_011511908.2:c.*223A>T	XP_011510210.1:n.*223A>T
XM_011511909.2:c.*223A>T	XP_011510211.1:n.*223A>T
XM_017005021.1:c.2435-6810A>T	XP_016860510.1:n.2435-6810A>T
XM_017005022.1:c.2473+258A>T	XP_016860511.1:n.2473+258A>T
XM_017005024.1:c.*223A>T	XP_016860513.1:n.*223A>T
XM_017005025.1:c.2319-6810A>T	XP_016860514.1:n.2319-6810A>T