Canonical Allele Identifier: CA339960329

Gene: SLC2A1

Linked Data

• MyVariant Identifiers: chr1:g.43396319A>G (hg19) ; chr1:g.42930648A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42930648A>G , CM000663.2:g.42930648A>G	GRCh38
NC_000001.10:g.43396319A>G , CM000663.1:g.43396319A>G	GRCh37
NC_000001.9:g.43168906A>G	NCBI36
NG_008232.1:g.33529T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.494T>C MANE Select	ENSP00000416293.2:p.Val165Ala
ENST00000674765.1:c.494T>C	ENSP00000501811.1:p.Val165Ala
ENST00000675112.1:n.517T>C
ENST00000676254.1:n.943T>C
ENST00000426263.7:c.494T>C	ENSP00000416293.2:p.Val165Ala
ENST00000439722.2:c.373T>C	ENSP00000395521.2:n.373T>C
ENST00000475162.3:c.393T>C
ENST00000625233.2:n.702T>C
ENST00000630287.2:c.494T>C	ENSP00000486694.1:p.Val165Ala
NM_006516.2:c.494T>C	NP_006507.2:p.Val165Ala
NM_006516.3:c.494T>C	NP_006507.2:p.Val165Ala
NM_006516.4:c.494T>C MANE Select	NP_006507.2:p.Val165Ala