Canonical Allele Identifier: CA363326032
Gene: AIF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31616102A>G , CM000668.2:g.31616102A>G GRCh38
NC_000006.11:g.31583879A>G , CM000668.1:g.31583879A>G GRCh37
NC_000006.10:g.31691858A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376059.8:c.155-2A>G MANE Select ENSP00000365227.3:n.155-2A>G
ENST00000337917.11:c.197-2A>G ENSP00000338776.7:n.197-2A>G
ENST00000376049.4:c.-10A>G ENSP00000365217.4:n.-10A>G
ENST00000376059.7:c.155-2A>G ENSP00000365227.3:n.155-2A>G
ENST00000466820.1:n.570A>G
ENST00000497362.5:n.572A>G
NM_001623.3:c.155-2A>G NP_001614.3:n.155-2A>G
NM_004847.3:c.-10A>G NP_004838.1:n.-10A>G
NM_032955.1:c.-10A>G NP_116573.1:n.-10A>G
XM_005248870.3:c.155-2A>G XP_005248927.1:n.155-2A>G
XM_005248871.1:c.218-2A>G XP_005248928.1:n.218-2A>G
NM_001318970.1:c.-8-2A>G NP_001305899.1:n.-8-2A>G
NM_001623.4:c.155-2A>G NP_001614.3:n.155-2A>G
NM_032955.2:c.-10A>G NP_116573.1:n.-10A>G
XM_005248870.4:c.155-2A>G XP_005248927.1:n.155-2A>G
XM_017010332.1:c.-8-2A>G XP_016865821.1:n.-8-2A>G
NM_001623.5:c.155-2A>G MANE Select NP_001614.3:n.155-2A>G
NM_001318970.2:c.-8-2A>G NP_001305899.1:n.-8-2A>G
NM_032955.3:c.-10A>G NP_116573.1:n.-10A>G