Canonical Allele Identifier: CA417543766

Gene: SLC2A1

Linked Data

• MyVariant Identifiers: chr1:g.43396393C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42930722C>G , CM000663.2:g.42930722C>G	GRCh38
NC_000001.10:g.43396393C>G , CM000663.1:g.43396393C>G	GRCh37
NC_000001.9:g.43168980C>G	NCBI36
NG_008232.1:g.33455G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.420G>C MANE Select	ENSP00000416293.2:p.Val140=
ENST00000674765.1:c.420G>C	ENSP00000501811.1:p.Val140=
ENST00000675112.1:n.443G>C
ENST00000676254.1:n.869G>C
ENST00000372500.4:c.324G>C	ENSP00000361578.4:p.Val108=
ENST00000426263.7:c.420G>C	ENSP00000416293.2:p.Val140=
ENST00000439722.2:c.299G>C	ENSP00000395521.2:n.299G>C
ENST00000475162.3:c.319G>C
ENST00000625233.2:n.628G>C
ENST00000630287.2:c.420G>C	ENSP00000486694.1:p.Val140=
NM_006516.2:c.420G>C	NP_006507.2:p.Val140=
NM_006516.3:c.420G>C	NP_006507.2:p.Val140=
NM_006516.4:c.420G>C MANE Select	NP_006507.2:p.Val140=