Canonical Allele Identifier: CA2677994790
Gene: AIF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31616094_31616095del , CM000668.2:g.31616094_31616095del GRCh38
NC_000006.11:g.31583871_31583872del , CM000668.1:g.31583871_31583872del GRCh37
NC_000006.10:g.31691850_31691851del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376059.8:c.155-10_155-9del MANE Select ENSP00000365227.3:n.155-10_155-9del
ENST00000337917.11:c.197-10_197-9del ENSP00000338776.7:n.197-10_197-9del
ENST00000376049.4:c.-18_-17del ENSP00000365217.4:n.-18_-17del
ENST00000376059.7:c.155-10_155-9del ENSP00000365227.3:n.155-10_155-9del
ENST00000466820.1:n.562_563del
ENST00000497362.5:n.564_565del
NM_001623.3:c.155-10_155-9del NP_001614.3:n.155-10_155-9del
NM_004847.3:c.-18_-17del NP_004838.1:n.-18_-17del
NM_032955.1:c.-18_-17del NP_116573.1:n.-18_-17del
XM_005248870.3:c.155-10_155-9del XP_005248927.1:n.155-10_155-9del
XM_005248871.1:c.218-10_218-9del XP_005248928.1:n.218-10_218-9del
NM_001318970.1:c.-8-10_-8-9del NP_001305899.1:n.-8-10_-8-9del
NM_001623.4:c.155-10_155-9del NP_001614.3:n.155-10_155-9del
NM_032955.2:c.-18_-17del NP_116573.1:n.-18_-17del
XM_005248870.4:c.155-10_155-9del XP_005248927.1:n.155-10_155-9del
XM_017010332.1:c.-8-10_-8-9del XP_016865821.1:n.-8-10_-8-9del
NM_001623.5:c.155-10_155-9del MANE Select NP_001614.3:n.155-10_155-9del
NM_001318970.2:c.-8-10_-8-9del NP_001305899.1:n.-8-10_-8-9del
NM_032955.3:c.-18_-17del NP_116573.1:n.-18_-17del