Canonical Allele Identifier: CA803378

Gene: SLC2A1

Linked Data

• dbSNP Id: rs773409073
• ExAC: 1:43394739 C / T
• gnomAD v2: 1-43394739-C-T
• gnomAD v4: 1-42929068-C-T
• MyVariant Identifiers: chr1:g.43394739C>T (hg19) ; chr1:g.42929068C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929068C>T , CM000663.2:g.42929068C>T	GRCh38
NC_000001.10:g.43394739C>T , CM000663.1:g.43394739C>T	GRCh37
NC_000001.9:g.43167326C>T	NCBI36
NG_008232.1:g.35109G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.973-35G>A MANE Select	ENSP00000416293.2:n.973-35G>A
ENST00000674545.1:n.432G>A
ENST00000674765.1:c.973-35G>A	ENSP00000501811.1:n.973-35G>A
ENST00000675112.1:n.1274-35G>A
ENST00000676254.1:n.1422-35G>A
ENST00000426263.7:c.973-35G>A	ENSP00000416293.2:n.973-35G>A
ENST00000439722.2:c.852-35G>A	ENSP00000395521.2:n.852-35G>A
ENST00000475162.3:c.415+1558G>A
ENST00000630287.2:c.*288-35G>A	ENSP00000486694.1:n.*288-35G>A
NM_006516.2:c.973-35G>A	NP_006507.2:n.973-35G>A
NM_006516.3:c.973-35G>A	NP_006507.2:n.973-35G>A
NM_006516.4:c.973-35G>A MANE Select	NP_006507.2:n.973-35G>A