Canonical Allele Identifier: CA1619230408

Gene: AIF1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31616161T= , CM000668.2:g.31616161T=	GRCh38
NC_000006.11:g.31583938T= , CM000668.1:g.31583938T=	GRCh37
NC_000006.10:g.31691917T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000376059.8:c.196+16T= MANE Select	ENSP00000365227.3:n.196+16T=
ENST00000337917.11:c.238+16T=	ENSP00000338776.7:n.238+16T=
ENST00000376049.4:c.34+16T=	ENSP00000365217.4:n.34+16T=
ENST00000376059.7:c.196+16T=	ENSP00000365227.3:n.196+16T=
ENST00000466820.1:n.629T=
ENST00000497362.5:n.631T=
NM_001623.3:c.196+16T=	NP_001614.3:n.196+16T=
NM_004847.3:c.50T=	NP_004838.1:p.Ile17=
NM_032955.1:c.34+16T=	NP_116573.1:n.34+16T=
XM_005248870.3:c.212T=	XP_005248927.1:p.Ile71=
XM_005248871.1:c.259+16T=	XP_005248928.1:n.259+16T=
NM_001318970.1:c.34+16T=	NP_001305899.1:n.34+16T=
NM_001623.4:c.196+16T=	NP_001614.3:n.196+16T=
NM_032955.2:c.34+16T=	NP_116573.1:n.34+16T=
XM_005248870.4:c.212T=	XP_005248927.1:p.Ile71=
XM_017010332.1:c.50T=	XP_016865821.1:p.Ile17=
NM_001623.5:c.196+16T= MANE Select	NP_001614.3:n.196+16T=
NM_001318970.2:c.34+16T=	NP_001305899.1:n.34+16T=
NM_032955.3:c.34+16T=	NP_116573.1:n.34+16T=