Canonical Allele Identifier: CA417409352

Gene: SLC2A1

Linked Data

• dbSNP Id: rs201996220
• MyVariant Identifiers: chr1:g.43395333G>C (hg19) ; chr1:g.42929662G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929662G>C , CM000663.2:g.42929662G>C	GRCh38
NC_000001.10:g.43395333G>C , CM000663.1:g.43395333G>C	GRCh37
NC_000001.9:g.43167920G>C	NCBI36
NG_008232.1:g.34515C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.798C>G MANE Select	ENSP00000416293.2:p.Pro266=
ENST00000669445.1:c.128C>G
ENST00000674765.1:c.798C>G	ENSP00000501811.1:p.Pro266=
ENST00000675112.1:n.821C>G
ENST00000676254.1:n.1247C>G
ENST00000426263.7:c.798C>G	ENSP00000416293.2:p.Pro266=
ENST00000439722.2:c.677C>G	ENSP00000395521.2:n.677C>G
ENST00000475162.3:c.415+964C>G
ENST00000630287.2:c.*113C>G	ENSP00000486694.1:n.*113C>G
NM_006516.2:c.798C>G	NP_006507.2:p.Pro266=
NM_006516.3:c.798C>G	NP_006507.2:p.Pro266=
NM_006516.4:c.798C>G MANE Select	NP_006507.2:p.Pro266=