Canonical Allele Identifier: CA417543389

Gene: SLC2A1

Linked Data

• MyVariant Identifiers: chr1:g.43395345C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929674C>A , CM000663.2:g.42929674C>A	GRCh38
NC_000001.10:g.43395345C>A , CM000663.1:g.43395345C>A	GRCh37
NC_000001.9:g.43167932C>A	NCBI36
NG_008232.1:g.34503G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.786G>T MANE Select	ENSP00000416293.2:p.Leu262=
ENST00000669445.1:c.116G>T
ENST00000674765.1:c.786G>T	ENSP00000501811.1:p.Leu262=
ENST00000675112.1:n.809G>T
ENST00000676254.1:n.1235G>T
ENST00000426263.7:c.786G>T	ENSP00000416293.2:p.Leu262=
ENST00000439722.2:c.665G>T	ENSP00000395521.2:n.665G>T
ENST00000475162.3:c.415+952G>T
ENST00000630287.2:c.*101G>T	ENSP00000486694.1:n.*101G>T
NM_006516.2:c.786G>T	NP_006507.2:p.Leu262=
NM_006516.3:c.786G>T	NP_006507.2:p.Leu262=
NM_006516.4:c.786G>T MANE Select	NP_006507.2:p.Leu262=