Canonical Allele Identifier: CA2645198921

Gene: SLC2A1

Linked Data

• gnomAD v4: 1-42929191-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929191C>T , CM000663.2:g.42929191C>T	GRCh38
NC_000001.10:g.43394862C>T , CM000663.1:g.43394862C>T	GRCh37
NC_000001.9:g.43167449C>T	NCBI36
NG_008232.1:g.34986G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.972+19G>A MANE Select	ENSP00000416293.2:n.972+19G>A
ENST00000674545.1:n.309G>A
ENST00000674765.1:c.972+19G>A	ENSP00000501811.1:n.972+19G>A
ENST00000675112.1:n.1273+19G>A
ENST00000676254.1:n.1421+19G>A
ENST00000426263.7:c.972+19G>A	ENSP00000416293.2:n.972+19G>A
ENST00000439722.2:c.851+19G>A	ENSP00000395521.2:n.851+19G>A
ENST00000475162.3:c.415+1435G>A
ENST00000630287.2:c.*287+19G>A	ENSP00000486694.1:n.*287+19G>A
NM_006516.2:c.972+19G>A	NP_006507.2:n.972+19G>A
NM_006516.3:c.972+19G>A	NP_006507.2:n.972+19G>A
NM_006516.4:c.972+19G>A MANE Select	NP_006507.2:n.972+19G>A