Canonical Allele Identifier: CA2677994873

Gene: AIF1

Linked Data

• gnomAD v4: 6-31616179-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31616179T>A , CM000668.2:g.31616179T>A	GRCh38
NC_000006.11:g.31583956T>A , CM000668.1:g.31583956T>A	GRCh37
NC_000006.10:g.31691935T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376059.8:c.196+34T>A MANE Select	ENSP00000365227.3:n.196+34T>A
ENST00000337917.11:c.238+34T>A	ENSP00000338776.7:n.238+34T>A
ENST00000376049.4:c.34+34T>A	ENSP00000365217.4:n.34+34T>A
ENST00000376059.7:c.196+34T>A	ENSP00000365227.3:n.196+34T>A
ENST00000466820.1:n.647T>A
ENST00000497362.5:n.649T>A
NM_001623.3:c.196+34T>A	NP_001614.3:n.196+34T>A
NM_004847.3:c.68T>A	NP_004838.1:p.Val23Glu
NM_032955.1:c.34+34T>A	NP_116573.1:n.34+34T>A
XM_005248870.3:c.230T>A	XP_005248927.1:p.Val77Glu
XM_005248871.1:c.259+34T>A	XP_005248928.1:n.259+34T>A
NM_001318970.1:c.34+34T>A	NP_001305899.1:n.34+34T>A
NM_001623.4:c.196+34T>A	NP_001614.3:n.196+34T>A
NM_032955.2:c.34+34T>A	NP_116573.1:n.34+34T>A
XM_005248870.4:c.230T>A	XP_005248927.1:p.Val77Glu
XM_017010332.1:c.68T>A	XP_016865821.1:p.Val23Glu
NM_001623.5:c.196+34T>A MANE Select	NP_001614.3:n.196+34T>A
NM_001318970.2:c.34+34T>A	NP_001305899.1:n.34+34T>A
NM_032955.3:c.34+34T>A	NP_116573.1:n.34+34T>A