Canonical Allele Identifier: CA339953869

Gene: SLC2A1

Linked Data

• MyVariant Identifiers: chr1:g.43393361C>G (hg19) ; chr1:g.42927690C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42927690C>G , CM000663.2:g.42927690C>G	GRCh38
NC_000001.10:g.43393361C>G , CM000663.1:g.43393361C>G	GRCh37
NC_000001.9:g.43165948C>G	NCBI36
NG_008232.1:g.36487G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.1193G>C MANE Select	ENSP00000416293.2:p.Gly398Ala
ENST00000674545.1:n.1810G>C
ENST00000674765.1:c.1030-833G>C	ENSP00000501811.1:n.1030-833G>C
ENST00000675112.1:n.1494G>C
ENST00000676254.1:n.1642G>C
ENST00000426263.7:c.1193G>C	ENSP00000416293.2:p.Gly398Ala
ENST00000475162.3:c.416-712G>C
ENST00000630287.2:c.*508G>C	ENSP00000486694.1:n.*508G>C
NM_006516.2:c.1193G>C	NP_006507.2:p.Gly398Ala
NM_006516.3:c.1193G>C	NP_006507.2:p.Gly398Ala
NM_006516.4:c.1193G>C MANE Select	NP_006507.2:p.Gly398Ala