Canonical Allele Identifier: CA2645198911
Gene: SLC2A1 HGNC NCBI

Linked Data

gnomAD v4: 1-42929165-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929165T>A , CM000663.2:g.42929165T>A GRCh38
NC_000001.10:g.43394836T>A , CM000663.1:g.43394836T>A GRCh37
NC_000001.9:g.43167423T>A NCBI36
NG_008232.1:g.35012A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.972+45A>T MANE Select ENSP00000416293.2:n.972+45A>T
ENST00000674545.1:n.335A>T
ENST00000674765.1:c.972+45A>T ENSP00000501811.1:n.972+45A>T
ENST00000675112.1:n.1273+45A>T
ENST00000676254.1:n.1421+45A>T
ENST00000426263.7:c.972+45A>T ENSP00000416293.2:n.972+45A>T
ENST00000439722.2:c.851+45A>T ENSP00000395521.2:n.851+45A>T
ENST00000475162.3:c.415+1461A>T
ENST00000630287.2:c.*287+45A>T ENSP00000486694.1:n.*287+45A>T
NM_006516.2:c.972+45A>T NP_006507.2:n.972+45A>T
NM_006516.3:c.972+45A>T NP_006507.2:n.972+45A>T
NM_006516.4:c.972+45A>T MANE Select NP_006507.2:n.972+45A>T