Canonical Allele Identifier: CA363326476

Gene: AIF1

Linked Data

• gnomAD v4: 6-31616142-A-G
• MyVariant Identifiers: chr6:g.31583919A>G (hg19) ; chr6:g.31616142A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31616142A>G , CM000668.2:g.31616142A>G	GRCh38
NC_000006.11:g.31583919A>G , CM000668.1:g.31583919A>G	GRCh37
NC_000006.10:g.31691898A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376059.8:c.193A>G MANE Select	ENSP00000365227.3:p.Ile65Val
ENST00000337917.11:c.235A>G	ENSP00000338776.7:p.Ile79Val
ENST00000376049.4:c.31A>G	ENSP00000365217.4:p.Ile11Val
ENST00000376059.7:c.193A>G	ENSP00000365227.3:p.Ile65Val
ENST00000466820.1:n.610A>G
ENST00000497362.5:n.612A>G
NM_001623.3:c.193A>G	NP_001614.3:p.Ile65Val
NM_004847.3:c.31A>G	NP_004838.1:p.Ile11Val
NM_032955.1:c.31A>G	NP_116573.1:p.Ile11Val
XM_005248870.3:c.193A>G	XP_005248927.1:p.Ile65Val
XM_005248871.1:c.256A>G	XP_005248928.1:p.Ile86Val
NM_001318970.1:c.31A>G	NP_001305899.1:p.Ile11Val
NM_001623.4:c.193A>G	NP_001614.3:p.Ile65Val
NM_032955.2:c.31A>G	NP_116573.1:p.Ile11Val
XM_005248870.4:c.193A>G	XP_005248927.1:p.Ile65Val
XM_017010332.1:c.31A>G	XP_016865821.1:p.Ile11Val
NM_001623.5:c.193A>G MANE Select	NP_001614.3:p.Ile65Val
NM_001318970.2:c.31A>G	NP_001305899.1:p.Ile11Val
NM_032955.3:c.31A>G	NP_116573.1:p.Ile11Val