Canonical Allele Identifier: CA1165412588
Gene: SLC2A1 HGNC NCBI

Linked Data

dbSNP Id: rs1643474848
gnomAD v4: 1-42930287-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930287G>T , CM000663.2:g.42930287G>T GRCh38
NC_000001.10:g.43395958G>T , CM000663.1:g.43395958G>T GRCh37
NC_000001.9:g.43168545G>T NCBI36
NG_008232.1:g.33890C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.517-252C>A MANE Select ENSP00000416293.2:n.517-252C>A
ENST00000674765.1:c.517-252C>A ENSP00000501811.1:n.517-252C>A
ENST00000675112.1:n.540-252C>A
ENST00000676254.1:n.966-252C>A
ENST00000426263.7:c.517-252C>A ENSP00000416293.2:n.517-252C>A
ENST00000439722.2:c.396-252C>A ENSP00000395521.2:n.396-252C>A
ENST00000475162.3:c.415+339C>A
ENST00000630287.2:c.516+339C>A ENSP00000486694.1:n.516+339C>A
NM_006516.2:c.517-252C>A NP_006507.2:n.517-252C>A
NM_006516.3:c.517-252C>A NP_006507.2:n.517-252C>A
NM_006516.4:c.517-252C>A MANE Select NP_006507.2:n.517-252C>A