Canonical Allele Identifier: CA363326279

Gene: AIF1

Linked Data

• MyVariant Identifiers: chr6:g.31583898G>A (hg19) ; chr6:g.31616121G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31616121G>A , CM000668.2:g.31616121G>A	GRCh38
NC_000006.11:g.31583898G>A , CM000668.1:g.31583898G>A	GRCh37
NC_000006.10:g.31691877G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376059.8:c.172G>A MANE Select	ENSP00000365227.3:p.Asp58Asn
ENST00000337917.11:c.214G>A	ENSP00000338776.7:p.Asp72Asn
ENST00000376049.4:c.10G>A	ENSP00000365217.4:p.Asp4Asn
ENST00000376059.7:c.172G>A	ENSP00000365227.3:p.Asp58Asn
ENST00000466820.1:n.589G>A
ENST00000497362.5:n.591G>A
NM_001623.3:c.172G>A	NP_001614.3:p.Asp58Asn
NM_004847.3:c.10G>A	NP_004838.1:p.Asp4Asn
NM_032955.1:c.10G>A	NP_116573.1:p.Asp4Asn
XM_005248870.3:c.172G>A	XP_005248927.1:p.Asp58Asn
XM_005248871.1:c.235G>A	XP_005248928.1:p.Asp79Asn
NM_001318970.1:c.10G>A	NP_001305899.1:p.Asp4Asn
NM_001623.4:c.172G>A	NP_001614.3:p.Asp58Asn
NM_032955.2:c.10G>A	NP_116573.1:p.Asp4Asn
XM_005248870.4:c.172G>A	XP_005248927.1:p.Asp58Asn
XM_017010332.1:c.10G>A	XP_016865821.1:p.Asp4Asn
NM_001623.5:c.172G>A MANE Select	NP_001614.3:p.Asp58Asn
NM_001318970.2:c.10G>A	NP_001305899.1:p.Asp4Asn
NM_032955.3:c.10G>A	NP_116573.1:p.Asp4Asn