Canonical Allele Identifier: CA2645198916

Gene: SLC2A1

Linked Data

• gnomAD v4: 1-42929181-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929181G>T , CM000663.2:g.42929181G>T	GRCh38
NC_000001.10:g.43394852G>T , CM000663.1:g.43394852G>T	GRCh37
NC_000001.9:g.43167439G>T	NCBI36
NG_008232.1:g.34996C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.972+29C>A MANE Select	ENSP00000416293.2:n.972+29C>A
ENST00000674545.1:n.319C>A
ENST00000674765.1:c.972+29C>A	ENSP00000501811.1:n.972+29C>A
ENST00000675112.1:n.1273+29C>A
ENST00000676254.1:n.1421+29C>A
ENST00000426263.7:c.972+29C>A	ENSP00000416293.2:n.972+29C>A
ENST00000439722.2:c.851+29C>A	ENSP00000395521.2:n.851+29C>A
ENST00000475162.3:c.415+1445C>A
ENST00000630287.2:c.*287+29C>A	ENSP00000486694.1:n.*287+29C>A
NM_006516.2:c.972+29C>A	NP_006507.2:n.972+29C>A
NM_006516.3:c.972+29C>A	NP_006507.2:n.972+29C>A
NM_006516.4:c.972+29C>A MANE Select	NP_006507.2:n.972+29C>A