Canonical Allele Identifier: CA1087479479
Gene: AIF1 HGNC NCBI

Linked Data

dbSNP Id: rs759432176
gnomAD v3: 6-31616175-G-A
gnomAD v4: 6-31616175-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31616175G>A , CM000668.2:g.31616175G>A GRCh38
NC_000006.11:g.31583952G>A , CM000668.1:g.31583952G>A GRCh37
NC_000006.10:g.31691931G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376059.8:c.196+30G>A MANE Select ENSP00000365227.3:n.196+30G>A
ENST00000337917.11:c.238+30G>A ENSP00000338776.7:n.238+30G>A
ENST00000376049.4:c.34+30G>A ENSP00000365217.4:n.34+30G>A
ENST00000376059.7:c.196+30G>A ENSP00000365227.3:n.196+30G>A
ENST00000466820.1:n.643G>A
ENST00000497362.5:n.645G>A
NM_001623.3:c.196+30G>A NP_001614.3:n.196+30G>A
NM_004847.3:c.64G>A NP_004838.1:p.Val22Met
NM_032955.1:c.34+30G>A NP_116573.1:n.34+30G>A
XM_005248870.3:c.226G>A XP_005248927.1:p.Val76Met
XM_005248871.1:c.259+30G>A XP_005248928.1:n.259+30G>A
NM_001318970.1:c.34+30G>A NP_001305899.1:n.34+30G>A
NM_001623.4:c.196+30G>A NP_001614.3:n.196+30G>A
NM_032955.2:c.34+30G>A NP_116573.1:n.34+30G>A
XM_005248870.4:c.226G>A XP_005248927.1:p.Val76Met
XM_017010332.1:c.64G>A XP_016865821.1:p.Val22Met
NM_001623.5:c.196+30G>A MANE Select NP_001614.3:n.196+30G>A
NM_001318970.2:c.34+30G>A NP_001305899.1:n.34+30G>A
NM_032955.3:c.34+30G>A NP_116573.1:n.34+30G>A