Canonical Allele Identifier: CA363326354
Gene: AIF1 HGNC NCBI

Linked Data

dbSNP Id: rs1482064144
gnomAD v2: 6-31583905-A-G
gnomAD v4: 6-31616128-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31616128A>G , CM000668.2:g.31616128A>G GRCh38
NC_000006.11:g.31583905A>G , CM000668.1:g.31583905A>G GRCh37
NC_000006.10:g.31691884A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376059.8:c.179A>G MANE Select ENSP00000365227.3:p.Asn60Ser
ENST00000337917.11:c.221A>G ENSP00000338776.7:p.Asn74Ser
ENST00000376049.4:c.17A>G ENSP00000365217.4:p.Asn6Ser
ENST00000376059.7:c.179A>G ENSP00000365227.3:p.Asn60Ser
ENST00000466820.1:n.596A>G
ENST00000497362.5:n.598A>G
NM_001623.3:c.179A>G NP_001614.3:p.Asn60Ser
NM_004847.3:c.17A>G NP_004838.1:p.Asn6Ser
NM_032955.1:c.17A>G NP_116573.1:p.Asn6Ser
XM_005248870.3:c.179A>G XP_005248927.1:p.Asn60Ser
XM_005248871.1:c.242A>G XP_005248928.1:p.Asn81Ser
NM_001318970.1:c.17A>G NP_001305899.1:p.Asn6Ser
NM_001623.4:c.179A>G NP_001614.3:p.Asn60Ser
NM_032955.2:c.17A>G NP_116573.1:p.Asn6Ser
XM_005248870.4:c.179A>G XP_005248927.1:p.Asn60Ser
XM_017010332.1:c.17A>G XP_016865821.1:p.Asn6Ser
NM_001623.5:c.179A>G MANE Select NP_001614.3:p.Asn60Ser
NM_001318970.2:c.17A>G NP_001305899.1:p.Asn6Ser
NM_032955.3:c.17A>G NP_116573.1:p.Asn6Ser