Canonical Allele Identifier: CA2677994779

Gene: AIF1

Linked Data

• gnomAD v4: 6-31616083-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31616084_31616085del , CM000668.2:g.31616084_31616085del	GRCh38
NC_000006.11:g.31583861_31583862del , CM000668.1:g.31583861_31583862del	GRCh37
NC_000006.10:g.31691840_31691841del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376059.8:c.155-20_155-19del MANE Select	ENSP00000365227.3:n.155-20_155-19del
ENST00000337917.11:c.197-20_197-19del	ENSP00000338776.7:n.197-20_197-19del
ENST00000376049.4:c.-28_-27del	ENSP00000365217.4:n.-28_-27del
ENST00000376059.7:c.155-20_155-19del	ENSP00000365227.3:n.155-20_155-19del
ENST00000466820.1:n.552_553del
ENST00000497362.5:n.554_555del
NM_001623.3:c.155-20_155-19del	NP_001614.3:n.155-20_155-19del
NM_004847.3:c.-28_-27del	NP_004838.1:n.-28_-27del
NM_032955.1:c.-28_-27del	NP_116573.1:n.-28_-27del
XM_005248870.3:c.155-20_155-19del	XP_005248927.1:n.155-20_155-19del
XM_005248871.1:c.218-20_218-19del	XP_005248928.1:n.218-20_218-19del
NM_001318970.1:c.-8-20_-8-19del	NP_001305899.1:n.-8-20_-8-19del
NM_001623.4:c.155-20_155-19del	NP_001614.3:n.155-20_155-19del
NM_032955.2:c.-28_-27del	NP_116573.1:n.-28_-27del
XM_005248870.4:c.155-20_155-19del	XP_005248927.1:n.155-20_155-19del
XM_017010332.1:c.-8-20_-8-19del	XP_016865821.1:n.-8-20_-8-19del
NM_001623.5:c.155-20_155-19del MANE Select	NP_001614.3:n.155-20_155-19del
NM_001318970.2:c.-8-20_-8-19del	NP_001305899.1:n.-8-20_-8-19del
NM_032955.3:c.-28_-27del	NP_116573.1:n.-28_-27del