Canonical Allele Identifier: CA21250993
Gene: SLC2A1 HGNC NCBI

Linked Data

dbSNP Id: rs145079633
gnomAD v3: 1-42929634-C-T
gnomAD v4: 1-42929634-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929634C>T , CM000663.2:g.42929634C>T GRCh38
NC_000001.10:g.43395305C>T , CM000663.1:g.43395305C>T GRCh37
NC_000001.9:g.43167892C>T NCBI36
NG_008232.1:g.34543G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.826G>A MANE Select ENSP00000416293.2:p.Val276Met
ENST00000674765.1:c.826G>A ENSP00000501811.1:p.Val276Met
ENST00000675112.1:n.849G>A
ENST00000676254.1:n.1275G>A
ENST00000426263.7:c.826G>A ENSP00000416293.2:p.Val276Met
ENST00000439722.2:c.705G>A ENSP00000395521.2:n.705G>A
ENST00000475162.3:c.415+992G>A
ENST00000630287.2:c.*141G>A ENSP00000486694.1:n.*141G>A
NM_006516.2:c.826G>A NP_006507.2:p.Val276Met
NM_006516.3:c.826G>A NP_006507.2:p.Val276Met
NM_006516.4:c.826G>A MANE Select NP_006507.2:p.Val276Met