Canonical Allele Identifier: CA2677994781
Gene: AIF1 HGNC NCBI

Linked Data

gnomAD v4: 6-31616086-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31616086C>A , CM000668.2:g.31616086C>A GRCh38
NC_000006.11:g.31583863C>A , CM000668.1:g.31583863C>A GRCh37
NC_000006.10:g.31691842C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376059.8:c.155-18C>A MANE Select ENSP00000365227.3:n.155-18C>A
ENST00000337917.11:c.197-18C>A ENSP00000338776.7:n.197-18C>A
ENST00000376049.4:c.-26C>A ENSP00000365217.4:n.-26C>A
ENST00000376059.7:c.155-18C>A ENSP00000365227.3:n.155-18C>A
ENST00000466820.1:n.554C>A
ENST00000497362.5:n.556C>A
NM_001623.3:c.155-18C>A NP_001614.3:n.155-18C>A
NM_004847.3:c.-26C>A NP_004838.1:n.-26C>A
NM_032955.1:c.-26C>A NP_116573.1:n.-26C>A
XM_005248870.3:c.155-18C>A XP_005248927.1:n.155-18C>A
XM_005248871.1:c.218-18C>A XP_005248928.1:n.218-18C>A
NM_001318970.1:c.-8-18C>A NP_001305899.1:n.-8-18C>A
NM_001623.4:c.155-18C>A NP_001614.3:n.155-18C>A
NM_032955.2:c.-26C>A NP_116573.1:n.-26C>A
XM_005248870.4:c.155-18C>A XP_005248927.1:n.155-18C>A
XM_017010332.1:c.-8-18C>A XP_016865821.1:n.-8-18C>A
NM_001623.5:c.155-18C>A MANE Select NP_001614.3:n.155-18C>A
NM_001318970.2:c.-8-18C>A NP_001305899.1:n.-8-18C>A
NM_032955.3:c.-26C>A NP_116573.1:n.-26C>A