Canonical Allele Identifier: CA339953067

Gene: SLC2A1

Linked Data

• dbSNP Id: rs2124445482
• MyVariant Identifiers: chr1:g.43392816T>A (hg19) ; chr1:g.42927145T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42927145T>A , CM000663.2:g.42927145T>A	GRCh38
NC_000001.10:g.43392816T>A , CM000663.1:g.43392816T>A	GRCh37
NC_000001.9:g.43165403T>A	NCBI36
NG_008232.1:g.37032A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.1375A>T MANE Select	ENSP00000416293.2:p.Thr459Ser
ENST00000674545.1:n.1992A>T
ENST00000674765.1:c.1030-288A>T	ENSP00000501811.1:n.1030-288A>T
ENST00000675112.1:n.1676A>T
ENST00000676254.1:n.1824A>T
ENST00000426263.7:c.1375A>T	ENSP00000416293.2:p.Thr459Ser
ENST00000475162.3:c.416-167A>T
ENST00000630287.2:c.*690A>T	ENSP00000486694.1:n.*690A>T
NM_006516.2:c.1375A>T	NP_006507.2:p.Thr459Ser
NM_006516.3:c.1375A>T	NP_006507.2:p.Thr459Ser
NM_006516.4:c.1375A>T MANE Select	NP_006507.2:p.Thr459Ser