Canonical Allele Identifier: CA363326363
Gene: AIF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31616131G>C , CM000668.2:g.31616131G>C GRCh38
NC_000006.11:g.31583908G>C , CM000668.1:g.31583908G>C GRCh37
NC_000006.10:g.31691887G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376059.8:c.182G>C MANE Select ENSP00000365227.3:p.Gly61Ala
ENST00000337917.11:c.224G>C ENSP00000338776.7:p.Gly75Ala
ENST00000376049.4:c.20G>C ENSP00000365217.4:p.Gly7Ala
ENST00000376059.7:c.182G>C ENSP00000365227.3:p.Gly61Ala
ENST00000466820.1:n.599G>C
ENST00000497362.5:n.601G>C
NM_001623.3:c.182G>C NP_001614.3:p.Gly61Ala
NM_004847.3:c.20G>C NP_004838.1:p.Gly7Ala
NM_032955.1:c.20G>C NP_116573.1:p.Gly7Ala
XM_005248870.3:c.182G>C XP_005248927.1:p.Gly61Ala
XM_005248871.1:c.245G>C XP_005248928.1:p.Gly82Ala
NM_001318970.1:c.20G>C NP_001305899.1:p.Gly7Ala
NM_001623.4:c.182G>C NP_001614.3:p.Gly61Ala
NM_032955.2:c.20G>C NP_116573.1:p.Gly7Ala
XM_005248870.4:c.182G>C XP_005248927.1:p.Gly61Ala
XM_017010332.1:c.20G>C XP_016865821.1:p.Gly7Ala
NM_001623.5:c.182G>C MANE Select NP_001614.3:p.Gly61Ala
NM_001318970.2:c.20G>C NP_001305899.1:p.Gly7Ala
NM_032955.3:c.20G>C NP_116573.1:p.Gly7Ala