Canonical Allele Identifier: CA735969591

Gene: SLC2A1

Linked Data

• dbSNP Id: rs1234081008
• gnomAD v3: 1-42929169-C-T
• gnomAD v4: 1-42929169-C-T
• MyVariant Identifiers: chr1:g.43394840C>T (hg19) ; chr1:g.42929169C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929169C>T , CM000663.2:g.42929169C>T	GRCh38
NC_000001.10:g.43394840C>T , CM000663.1:g.43394840C>T	GRCh37
NC_000001.9:g.43167427C>T	NCBI36
NG_008232.1:g.35008G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.972+41G>A MANE Select	ENSP00000416293.2:n.972+41G>A
ENST00000674545.1:n.331G>A
ENST00000674765.1:c.972+41G>A	ENSP00000501811.1:n.972+41G>A
ENST00000675112.1:n.1273+41G>A
ENST00000676254.1:n.1421+41G>A
ENST00000426263.7:c.972+41G>A	ENSP00000416293.2:n.972+41G>A
ENST00000439722.2:c.851+41G>A	ENSP00000395521.2:n.851+41G>A
ENST00000475162.3:c.415+1457G>A
ENST00000630287.2:c.*287+41G>A	ENSP00000486694.1:n.*287+41G>A
NM_006516.2:c.972+41G>A	NP_006507.2:n.972+41G>A
NM_006516.3:c.972+41G>A	NP_006507.2:n.972+41G>A
NM_006516.4:c.972+41G>A MANE Select	NP_006507.2:n.972+41G>A