Canonical Allele Identifier: CA363326215

Gene: AIF1

Linked Data

• MyVariant Identifiers: chr6:g.31583893A>T (hg19) ; chr6:g.31616116A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31616116A>T , CM000668.2:g.31616116A>T	GRCh38
NC_000006.11:g.31583893A>T , CM000668.1:g.31583893A>T	GRCh37
NC_000006.10:g.31691872A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376059.8:c.167A>T MANE Select	ENSP00000365227.3:p.Glu56Val
ENST00000337917.11:c.209A>T	ENSP00000338776.7:p.Glu70Val
ENST00000376049.4:c.5A>T	ENSP00000365217.4:p.Glu2Val
ENST00000376059.7:c.167A>T	ENSP00000365227.3:p.Glu56Val
ENST00000466820.1:n.584A>T
ENST00000497362.5:n.586A>T
NM_001623.3:c.167A>T	NP_001614.3:p.Glu56Val
NM_004847.3:c.5A>T	NP_004838.1:p.Glu2Val
NM_032955.1:c.5A>T	NP_116573.1:p.Glu2Val
XM_005248870.3:c.167A>T	XP_005248927.1:p.Glu56Val
XM_005248871.1:c.230A>T	XP_005248928.1:p.Glu77Val
NM_001318970.1:c.5A>T	NP_001305899.1:p.Glu2Val
NM_001623.4:c.167A>T	NP_001614.3:p.Glu56Val
NM_032955.2:c.5A>T	NP_116573.1:p.Glu2Val
XM_005248870.4:c.167A>T	XP_005248927.1:p.Glu56Val
XM_017010332.1:c.5A>T	XP_016865821.1:p.Glu2Val
NM_001623.5:c.167A>T MANE Select	NP_001614.3:p.Glu56Val
NM_001318970.2:c.5A>T	NP_001305899.1:p.Glu2Val
NM_032955.3:c.5A>T	NP_116573.1:p.Glu2Val