Canonical Allele Identifier: CA522496623

Gene: SLC2A1

Linked Data

• dbSNP Id: rs1251048149
• gnomAD v2: 1-43396059-G-A
• gnomAD v3: 1-42930388-G-A
• gnomAD v4: 1-42930388-G-A
• MyVariant Identifiers: chr1:g.43396059G>A (hg19) ; chr1:g.42930388G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42930388G>A , CM000663.2:g.42930388G>A	GRCh38
NC_000001.10:g.43396059G>A , CM000663.1:g.43396059G>A	GRCh37
NC_000001.9:g.43168646G>A	NCBI36
NG_008232.1:g.33789C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.516+238C>T MANE Select	ENSP00000416293.2:n.516+238C>T
ENST00000674765.1:c.516+238C>T	ENSP00000501811.1:n.516+238C>T
ENST00000675112.1:n.539+238C>T
ENST00000676254.1:n.965+238C>T
ENST00000426263.7:c.516+238C>T	ENSP00000416293.2:n.516+238C>T
ENST00000439722.2:c.395+238C>T	ENSP00000395521.2:n.395+238C>T
ENST00000475162.3:c.415+238C>T
ENST00000625233.2:n.962C>T
ENST00000630287.2:c.516+238C>T	ENSP00000486694.1:n.516+238C>T
NM_006516.2:c.516+238C>T	NP_006507.2:n.516+238C>T
NM_006516.3:c.516+238C>T	NP_006507.2:n.516+238C>T
NM_006516.4:c.516+238C>T MANE Select	NP_006507.2:n.516+238C>T