Canonical Allele Identifier: CA1619230396

Gene: AIF1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31616124C= , CM000668.2:g.31616124C=	GRCh38
NC_000006.11:g.31583901C= , CM000668.1:g.31583901C=	GRCh37
NC_000006.10:g.31691880C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376059.8:c.175C= MANE Select	ENSP00000365227.3:p.Leu59=
ENST00000337917.11:c.217C=	ENSP00000338776.7:p.Leu73=
ENST00000376049.4:c.13C=	ENSP00000365217.4:p.Leu5=
ENST00000376059.7:c.175C=	ENSP00000365227.3:p.Leu59=
ENST00000466820.1:n.592C=
ENST00000497362.5:n.594C=
NM_001623.3:c.175C=	NP_001614.3:p.Leu59=
NM_004847.3:c.13C=	NP_004838.1:p.Leu5=
NM_032955.1:c.13C=	NP_116573.1:p.Leu5=
XM_005248870.3:c.175C=	XP_005248927.1:p.Leu59=
XM_005248871.1:c.238C=	XP_005248928.1:p.Leu80=
NM_001318970.1:c.13C=	NP_001305899.1:p.Leu5=
NM_001623.4:c.175C=	NP_001614.3:p.Leu59=
NM_032955.2:c.13C=	NP_116573.1:p.Leu5=
XM_005248870.4:c.175C=	XP_005248927.1:p.Leu59=
XM_017010332.1:c.13C=	XP_016865821.1:p.Leu5=
NM_001623.5:c.175C= MANE Select	NP_001614.3:p.Leu59=
NM_001318970.2:c.13C=	NP_001305899.1:p.Leu5=
NM_032955.3:c.13C=	NP_116573.1:p.Leu5=