Canonical Allele Identifier: CA363326392
Gene: AIF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31616133A>T , CM000668.2:g.31616133A>T GRCh38
NC_000006.11:g.31583910A>T , CM000668.1:g.31583910A>T GRCh37
NC_000006.10:g.31691889A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376059.8:c.184A>T MANE Select ENSP00000365227.3:p.Asn62Tyr
ENST00000337917.11:c.226A>T ENSP00000338776.7:p.Asn76Tyr
ENST00000376049.4:c.22A>T ENSP00000365217.4:p.Asn8Tyr
ENST00000376059.7:c.184A>T ENSP00000365227.3:p.Asn62Tyr
ENST00000466820.1:n.601A>T
ENST00000497362.5:n.603A>T
NM_001623.3:c.184A>T NP_001614.3:p.Asn62Tyr
NM_004847.3:c.22A>T NP_004838.1:p.Asn8Tyr
NM_032955.1:c.22A>T NP_116573.1:p.Asn8Tyr
XM_005248870.3:c.184A>T XP_005248927.1:p.Asn62Tyr
XM_005248871.1:c.247A>T XP_005248928.1:p.Asn83Tyr
NM_001318970.1:c.22A>T NP_001305899.1:p.Asn8Tyr
NM_001623.4:c.184A>T NP_001614.3:p.Asn62Tyr
NM_032955.2:c.22A>T NP_116573.1:p.Asn8Tyr
XM_005248870.4:c.184A>T XP_005248927.1:p.Asn62Tyr
XM_017010332.1:c.22A>T XP_016865821.1:p.Asn8Tyr
NM_001623.5:c.184A>T MANE Select NP_001614.3:p.Asn62Tyr
NM_001318970.2:c.22A>T NP_001305899.1:p.Asn8Tyr
NM_032955.3:c.22A>T NP_116573.1:p.Asn8Tyr