Canonical Allele Identifier: CA449661624

Gene: AIF1

Linked Data

• MyVariant Identifiers: chr6:g.31583921T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31616144T>C , CM000668.2:g.31616144T>C	GRCh38
NC_000006.11:g.31583921T>C , CM000668.1:g.31583921T>C	GRCh37
NC_000006.10:g.31691900T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376059.8:c.195T>C MANE Select	ENSP00000365227.3:p.Ile65=
ENST00000337917.11:c.237T>C	ENSP00000338776.7:p.Ile79=
ENST00000376049.4:c.33T>C	ENSP00000365217.4:p.Ile11=
ENST00000376059.7:c.195T>C	ENSP00000365227.3:p.Ile65=
ENST00000466820.1:n.612T>C
ENST00000497362.5:n.614T>C
NM_001623.3:c.195T>C	NP_001614.3:p.Ile65=
NM_004847.3:c.33T>C	NP_004838.1:p.Ile11=
NM_032955.1:c.33T>C	NP_116573.1:p.Ile11=
XM_005248870.3:c.195T>C	XP_005248927.1:p.Ile65=
XM_005248871.1:c.258T>C	XP_005248928.1:p.Ile86=
NM_001318970.1:c.33T>C	NP_001305899.1:p.Ile11=
NM_001623.4:c.195T>C	NP_001614.3:p.Ile65=
NM_032955.2:c.33T>C	NP_116573.1:p.Ile11=
XM_005248870.4:c.195T>C	XP_005248927.1:p.Ile65=
XM_017010332.1:c.33T>C	XP_016865821.1:p.Ile11=
NM_001623.5:c.195T>C MANE Select	NP_001614.3:p.Ile65=
NM_001318970.2:c.33T>C	NP_001305899.1:p.Ile11=
NM_032955.3:c.33T>C	NP_116573.1:p.Ile11=