Canonical Allele Identifier: CA339958170

Gene: SLC2A1

Linked Data

• dbSNP Id: rs1643467472
• gnomAD v3: 1-42929747-G-A
• gnomAD v4: 1-42929747-G-A
• MyVariant Identifiers: chr1:g.43395418G>A (hg19) ; chr1:g.42929747G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929747G>A , CM000663.2:g.42929747G>A	GRCh38
NC_000001.10:g.43395418G>A , CM000663.1:g.43395418G>A	GRCh37
NC_000001.9:g.43168005G>A	NCBI36
NG_008232.1:g.34430C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.713C>T MANE Select	ENSP00000416293.2:p.Thr238Ile
ENST00000669445.1:c.57-14C>T
ENST00000674765.1:c.713C>T	ENSP00000501811.1:p.Thr238Ile
ENST00000675112.1:n.736C>T
ENST00000676254.1:n.1162C>T
ENST00000426263.7:c.713C>T	ENSP00000416293.2:p.Thr238Ile
ENST00000439722.2:c.592C>T	ENSP00000395521.2:n.592C>T
ENST00000475162.3:c.415+879C>T
ENST00000630287.2:c.*28C>T	ENSP00000486694.1:n.*28C>T
NM_006516.2:c.713C>T	NP_006507.2:p.Thr238Ile
NM_006516.3:c.713C>T	NP_006507.2:p.Thr238Ile
NM_006516.4:c.713C>T MANE Select	NP_006507.2:p.Thr238Ile