Canonical Allele Identifier: CA417543778
Gene: SLC2A1 HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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