Canonical Allele Identifier: CA363326495
Gene: AIF1 HGNC NCBI

Linked Data

dbSNP Id: rs1774332068

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31616143T>A , CM000668.2:g.31616143T>A GRCh38
NC_000006.11:g.31583920T>A , CM000668.1:g.31583920T>A GRCh37
NC_000006.10:g.31691899T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376059.8:c.194T>A MANE Select ENSP00000365227.3:p.Ile65Asn
ENST00000337917.11:c.236T>A ENSP00000338776.7:p.Ile79Asn
ENST00000376049.4:c.32T>A ENSP00000365217.4:p.Ile11Asn
ENST00000376059.7:c.194T>A ENSP00000365227.3:p.Ile65Asn
ENST00000466820.1:n.611T>A
ENST00000497362.5:n.613T>A
NM_001623.3:c.194T>A NP_001614.3:p.Ile65Asn
NM_004847.3:c.32T>A NP_004838.1:p.Ile11Asn
NM_032955.1:c.32T>A NP_116573.1:p.Ile11Asn
XM_005248870.3:c.194T>A XP_005248927.1:p.Ile65Asn
XM_005248871.1:c.257T>A XP_005248928.1:p.Ile86Asn
NM_001318970.1:c.32T>A NP_001305899.1:p.Ile11Asn
NM_001623.4:c.194T>A NP_001614.3:p.Ile65Asn
NM_032955.2:c.32T>A NP_116573.1:p.Ile11Asn
XM_005248870.4:c.194T>A XP_005248927.1:p.Ile65Asn
XM_017010332.1:c.32T>A XP_016865821.1:p.Ile11Asn
NM_001623.5:c.194T>A MANE Select NP_001614.3:p.Ile65Asn
NM_001318970.2:c.32T>A NP_001305899.1:p.Ile11Asn
NM_032955.3:c.32T>A NP_116573.1:p.Ile11Asn