Canonical Allele Identifier: CA1619230399

Gene: AIF1

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376059.8:c.181G= MANE Select	ENSP00000365227.3:p.Gly61=
ENST00000337917.11:c.223G=	ENSP00000338776.7:p.Gly75=
ENST00000376049.4:c.19G=	ENSP00000365217.4:p.Gly7=
ENST00000376059.7:c.181G=	ENSP00000365227.3:p.Gly61=
ENST00000466820.1:n.598G=
ENST00000497362.5:n.600G=
NM_001623.3:c.181G=	NP_001614.3:p.Gly61=
NM_004847.3:c.19G=	NP_004838.1:p.Gly7=
NM_032955.1:c.19G=	NP_116573.1:p.Gly7=
XM_005248870.3:c.181G=	XP_005248927.1:p.Gly61=
XM_005248871.1:c.244G=	XP_005248928.1:p.Gly82=
NM_001318970.1:c.19G=	NP_001305899.1:p.Gly7=
NM_001623.4:c.181G=	NP_001614.3:p.Gly61=
NM_032955.2:c.19G=	NP_116573.1:p.Gly7=
XM_005248870.4:c.181G=	XP_005248927.1:p.Gly61=
XM_017010332.1:c.19G=	XP_016865821.1:p.Gly7=
NM_001623.5:c.181G= MANE Select	NP_001614.3:p.Gly61=
NM_001318970.2:c.19G=	NP_001305899.1:p.Gly7=
NM_032955.3:c.19G=	NP_116573.1:p.Gly7=