Canonical Allele Identifier: CA136845680
Gene: AIF1 HGNC NCBI

Linked Data

dbSNP Id: rs899547810

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31616137G>C , CM000668.2:g.31616137G>C GRCh38
NC_000006.11:g.31583914G>C , CM000668.1:g.31583914G>C GRCh37
NC_000006.10:g.31691893G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376059.8:c.188G>C MANE Select ENSP00000365227.3:p.Gly63Ala
ENST00000337917.11:c.230G>C ENSP00000338776.7:p.Gly77Ala
ENST00000376049.4:c.26G>C ENSP00000365217.4:p.Gly9Ala
ENST00000376059.7:c.188G>C ENSP00000365227.3:p.Gly63Ala
ENST00000466820.1:n.605G>C
ENST00000497362.5:n.607G>C
NM_001623.3:c.188G>C NP_001614.3:p.Gly63Ala
NM_004847.3:c.26G>C NP_004838.1:p.Gly9Ala
NM_032955.1:c.26G>C NP_116573.1:p.Gly9Ala
XM_005248870.3:c.188G>C XP_005248927.1:p.Gly63Ala
XM_005248871.1:c.251G>C XP_005248928.1:p.Gly84Ala
NM_001318970.1:c.26G>C NP_001305899.1:p.Gly9Ala
NM_001623.4:c.188G>C NP_001614.3:p.Gly63Ala
NM_032955.2:c.26G>C NP_116573.1:p.Gly9Ala
XM_005248870.4:c.188G>C XP_005248927.1:p.Gly63Ala
XM_017010332.1:c.26G>C XP_016865821.1:p.Gly9Ala
NM_001623.5:c.188G>C MANE Select NP_001614.3:p.Gly63Ala
NM_001318970.2:c.26G>C NP_001305899.1:p.Gly9Ala
NM_032955.3:c.26G>C NP_116573.1:p.Gly9Ala