Canonical Allele Identifier: CA339960679

Gene: SLC2A1

Linked Data

• MyVariant Identifiers: chr1:g.43396379C>T (hg19) ; chr1:g.42930708C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42930708C>T , CM000663.2:g.42930708C>T	GRCh38
NC_000001.10:g.43396379C>T , CM000663.1:g.43396379C>T	GRCh37
NC_000001.9:g.43168966C>T	NCBI36
NG_008232.1:g.33469G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.434G>A MANE Select	ENSP00000416293.2:p.Gly145Asp
ENST00000674765.1:c.434G>A	ENSP00000501811.1:p.Gly145Asp
ENST00000675112.1:n.457G>A
ENST00000676254.1:n.883G>A
ENST00000372500.4:c.338G>A	ENSP00000361578.4:p.Gly113Asp
ENST00000426263.7:c.434G>A	ENSP00000416293.2:p.Gly145Asp
ENST00000439722.2:c.313G>A	ENSP00000395521.2:n.313G>A
ENST00000475162.3:c.333G>A
ENST00000625233.2:n.642G>A
ENST00000630287.2:c.434G>A	ENSP00000486694.1:p.Gly145Asp
NM_006516.2:c.434G>A	NP_006507.2:p.Gly145Asp
NM_006516.3:c.434G>A	NP_006507.2:p.Gly145Asp
NM_006516.4:c.434G>A MANE Select	NP_006507.2:p.Gly145Asp