Canonical Allele Identifier: CA2645198914

Gene: SLC2A1

Linked Data

• gnomAD v4: 1-42929172-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929172T>C , CM000663.2:g.42929172T>C	GRCh38
NC_000001.10:g.43394843T>C , CM000663.1:g.43394843T>C	GRCh37
NC_000001.9:g.43167430T>C	NCBI36
NG_008232.1:g.35005A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.972+38A>G MANE Select	ENSP00000416293.2:n.972+38A>G
ENST00000674545.1:n.328A>G
ENST00000674765.1:c.972+38A>G	ENSP00000501811.1:n.972+38A>G
ENST00000675112.1:n.1273+38A>G
ENST00000676254.1:n.1421+38A>G
ENST00000426263.7:c.972+38A>G	ENSP00000416293.2:n.972+38A>G
ENST00000439722.2:c.851+38A>G	ENSP00000395521.2:n.851+38A>G
ENST00000475162.3:c.415+1454A>G
ENST00000630287.2:c.*287+38A>G	ENSP00000486694.1:n.*287+38A>G
NM_006516.2:c.972+38A>G	NP_006507.2:n.972+38A>G
NM_006516.3:c.972+38A>G	NP_006507.2:n.972+38A>G
NM_006516.4:c.972+38A>G MANE Select	NP_006507.2:n.972+38A>G