Canonical Allele Identifier: CA3714799

Gene: AIF1

Linked Data

• dbSNP Id: rs764975742
• ExAC: 6:31583957 G / A
• gnomAD v2: 6-31583957-G-A
• gnomAD v3: 6-31616180-G-A
• gnomAD v4: 6-31616180-G-A
• MyVariant Identifiers: chr6:g.31583957G>A (hg19) ; chr6:g.31616180G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31616180G>A , CM000668.2:g.31616180G>A	GRCh38
NC_000006.11:g.31583957G>A , CM000668.1:g.31583957G>A	GRCh37
NC_000006.10:g.31691936G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000376059.8:c.196+35G>A MANE Select	ENSP00000365227.3:n.196+35G>A
ENST00000337917.11:c.238+35G>A	ENSP00000338776.7:n.238+35G>A
ENST00000376049.4:c.34+35G>A	ENSP00000365217.4:n.34+35G>A
ENST00000376059.7:c.196+35G>A	ENSP00000365227.3:n.196+35G>A
ENST00000466820.1:n.648G>A
ENST00000497362.5:n.650G>A
NM_001623.3:c.196+35G>A	NP_001614.3:n.196+35G>A
NM_004847.3:c.69G>A	NP_004838.1:p.Val23=
NM_032955.1:c.34+35G>A	NP_116573.1:n.34+35G>A
XM_005248870.3:c.231G>A	XP_005248927.1:p.Val77=
XM_005248871.1:c.259+35G>A	XP_005248928.1:n.259+35G>A
NM_001318970.1:c.34+35G>A	NP_001305899.1:n.34+35G>A
NM_001623.4:c.196+35G>A	NP_001614.3:n.196+35G>A
NM_032955.2:c.34+35G>A	NP_116573.1:n.34+35G>A
XM_005248870.4:c.231G>A	XP_005248927.1:p.Val77=
XM_017010332.1:c.69G>A	XP_016865821.1:p.Val23=
NM_001623.5:c.196+35G>A MANE Select	NP_001614.3:n.196+35G>A
NM_001318970.2:c.34+35G>A	NP_001305899.1:n.34+35G>A
NM_032955.3:c.34+35G>A	NP_116573.1:n.34+35G>A