Canonical Allele Identifier: CA449661600

Gene: AIF1

Linked Data

• gnomAD v4: 6-31616123-C-T
• MyVariant Identifiers: chr6:g.31583900C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31616123C>T , CM000668.2:g.31616123C>T	GRCh38
NC_000006.11:g.31583900C>T , CM000668.1:g.31583900C>T	GRCh37
NC_000006.10:g.31691879C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376059.8:c.174C>T MANE Select	ENSP00000365227.3:p.Asp58=
ENST00000337917.11:c.216C>T	ENSP00000338776.7:p.Asp72=
ENST00000376049.4:c.12C>T	ENSP00000365217.4:p.Asp4=
ENST00000376059.7:c.174C>T	ENSP00000365227.3:p.Asp58=
ENST00000466820.1:n.591C>T
ENST00000497362.5:n.593C>T
NM_001623.3:c.174C>T	NP_001614.3:p.Asp58=
NM_004847.3:c.12C>T	NP_004838.1:p.Asp4=
NM_032955.1:c.12C>T	NP_116573.1:p.Asp4=
XM_005248870.3:c.174C>T	XP_005248927.1:p.Asp58=
XM_005248871.1:c.237C>T	XP_005248928.1:p.Asp79=
NM_001318970.1:c.12C>T	NP_001305899.1:p.Asp4=
NM_001623.4:c.174C>T	NP_001614.3:p.Asp58=
NM_032955.2:c.12C>T	NP_116573.1:p.Asp4=
XM_005248870.4:c.174C>T	XP_005248927.1:p.Asp58=
XM_017010332.1:c.12C>T	XP_016865821.1:p.Asp4=
NM_001623.5:c.174C>T MANE Select	NP_001614.3:p.Asp58=
NM_001318970.2:c.12C>T	NP_001305899.1:p.Asp4=
NM_032955.3:c.12C>T	NP_116573.1:p.Asp4=