Canonical Allele Identifier: CA339956746

Gene: SLC2A1

Linked Data

• dbSNP Id: rs1570592136
• MyVariant Identifiers: chr1:g.43394945A>C (hg19) ; chr1:g.42929274A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929274A>C , CM000663.2:g.42929274A>C	GRCh38
NC_000001.10:g.43394945A>C , CM000663.1:g.43394945A>C	GRCh37
NC_000001.9:g.43167532A>C	NCBI36
NG_008232.1:g.34903T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.908T>G MANE Select	ENSP00000416293.2:p.Val303Gly
ENST00000674545.1:n.226T>G
ENST00000674765.1:c.908T>G	ENSP00000501811.1:p.Val303Gly
ENST00000675112.1:n.1209T>G
ENST00000676254.1:n.1357T>G
ENST00000426263.7:c.908T>G	ENSP00000416293.2:p.Val303Gly
ENST00000439722.2:c.787T>G	ENSP00000395521.2:n.787T>G
ENST00000475162.3:c.415+1352T>G
ENST00000630287.2:c.*223T>G	ENSP00000486694.1:n.*223T>G
NM_006516.2:c.908T>G	NP_006507.2:p.Val303Gly
NM_006516.3:c.908T>G	NP_006507.2:p.Val303Gly
NM_006516.4:c.908T>G MANE Select	NP_006507.2:p.Val303Gly