Canonical Allele Identifier: CA417543780

Gene: SLC2A1

Linked Data

• gnomAD v4: 1-42930728-G-T
• MyVariant Identifiers: chr1:g.43396399G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42930728G>T , CM000663.2:g.42930728G>T	GRCh38
NC_000001.10:g.43396399G>T , CM000663.1:g.43396399G>T	GRCh37
NC_000001.9:g.43168986G>T	NCBI36
NG_008232.1:g.33449C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.414C>A MANE Select	ENSP00000416293.2:p.Gly138=
ENST00000674765.1:c.414C>A	ENSP00000501811.1:p.Gly138=
ENST00000675112.1:n.437C>A
ENST00000676254.1:n.863C>A
ENST00000372500.4:c.318C>A	ENSP00000361578.4:p.Gly106=
ENST00000426263.7:c.414C>A	ENSP00000416293.2:p.Gly138=
ENST00000439722.2:c.293C>A	ENSP00000395521.2:n.293C>A
ENST00000475162.3:c.313C>A
ENST00000625233.2:n.622C>A
ENST00000630287.2:c.414C>A	ENSP00000486694.1:p.Gly138=
NM_006516.2:c.414C>A	NP_006507.2:p.Gly138=
NM_006516.3:c.414C>A	NP_006507.2:p.Gly138=
NM_006516.4:c.414C>A MANE Select	NP_006507.2:p.Gly138=