Canonical Allele Identifier: CA417409009

Gene: SLC2A1

Linked Data

• MyVariant Identifiers: chr1:g.43394899C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929228C>G , CM000663.2:g.42929228C>G	GRCh38
NC_000001.10:g.43394899C>G , CM000663.1:g.43394899C>G	GRCh37
NC_000001.9:g.43167486C>G	NCBI36
NG_008232.1:g.34949G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.954G>C MANE Select	ENSP00000416293.2:p.Thr318=
ENST00000674545.1:n.272G>C
ENST00000674765.1:c.954G>C	ENSP00000501811.1:p.Thr318=
ENST00000675112.1:n.1255G>C
ENST00000676254.1:n.1403G>C
ENST00000426263.7:c.954G>C	ENSP00000416293.2:p.Thr318=
ENST00000439722.2:c.833G>C	ENSP00000395521.2:n.833G>C
ENST00000475162.3:c.415+1398G>C
ENST00000630287.2:c.*269G>C	ENSP00000486694.1:n.*269G>C
NM_006516.2:c.954G>C	NP_006507.2:p.Thr318=
NM_006516.3:c.954G>C	NP_006507.2:p.Thr318=
NM_006516.4:c.954G>C MANE Select	NP_006507.2:p.Thr318=