Canonical Allele Identifier: CA3714788

Gene: AIF1

Linked Data

• dbSNP Id: rs781443488
• ExAC: 6:31583907 G / A
• gnomAD v2: 6-31583907-G-A
• gnomAD v3: 6-31616130-G-A
• gnomAD v4: 6-31616130-G-A
• MyVariant Identifiers: chr6:g.31583907G>A (hg19) ; chr6:g.31616130G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31616130G>A , CM000668.2:g.31616130G>A	GRCh38
NC_000006.11:g.31583907G>A , CM000668.1:g.31583907G>A	GRCh37
NC_000006.10:g.31691886G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376059.8:c.181G>A MANE Select	ENSP00000365227.3:p.Gly61Arg
ENST00000337917.11:c.223G>A	ENSP00000338776.7:p.Gly75Arg
ENST00000376049.4:c.19G>A	ENSP00000365217.4:p.Gly7Arg
ENST00000376059.7:c.181G>A	ENSP00000365227.3:p.Gly61Arg
ENST00000466820.1:n.598G>A
ENST00000497362.5:n.600G>A
NM_001623.3:c.181G>A	NP_001614.3:p.Gly61Arg
NM_004847.3:c.19G>A	NP_004838.1:p.Gly7Arg
NM_032955.1:c.19G>A	NP_116573.1:p.Gly7Arg
XM_005248870.3:c.181G>A	XP_005248927.1:p.Gly61Arg
XM_005248871.1:c.244G>A	XP_005248928.1:p.Gly82Arg
NM_001318970.1:c.19G>A	NP_001305899.1:p.Gly7Arg
NM_001623.4:c.181G>A	NP_001614.3:p.Gly61Arg
NM_032955.2:c.19G>A	NP_116573.1:p.Gly7Arg
XM_005248870.4:c.181G>A	XP_005248927.1:p.Gly61Arg
XM_017010332.1:c.19G>A	XP_016865821.1:p.Gly7Arg
NM_001623.5:c.181G>A MANE Select	NP_001614.3:p.Gly61Arg
NM_001318970.2:c.19G>A	NP_001305899.1:p.Gly7Arg
NM_032955.3:c.19G>A	NP_116573.1:p.Gly7Arg