Canonical Allele Identifier: CA363326026
Gene: AIF1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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