Canonical Allele Identifier: CA735978132

Gene: SLC2A1

Linked Data

• dbSNP Id: rs1219009199
• gnomAD v4: 1-42943370-A-G
• MyVariant Identifiers: chr1:g.43409041A>G (hg19) ; chr1:g.42943370A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42943370A>G , CM000663.2:g.42943370A>G	GRCh38
NC_000001.10:g.43409041A>G , CM000663.1:g.43409041A>G	GRCh37
NC_000001.9:g.43181628A>G	NCBI36
NG_008232.1:g.20807T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.19-49T>C MANE Select	ENSP00000416293.2:n.19-49T>C
ENST00000674765.1:c.19-49T>C	ENSP00000501811.1:n.19-49T>C
ENST00000675112.1:n.42-49T>C
ENST00000372500.4:c.19-12164T>C	ENSP00000361578.4:n.19-12164T>C
ENST00000415851.6:n.236-49T>C
ENST00000426263.7:c.19-49T>C	ENSP00000416293.2:n.19-49T>C
ENST00000625233.2:n.227-49T>C
ENST00000628173.1:n.238-49T>C
ENST00000630287.2:c.19-49T>C	ENSP00000486694.1:n.19-49T>C
ENST00000630821.1:n.236-49T>C
NM_006516.2:c.19-49T>C	NP_006507.2:n.19-49T>C
NM_006516.3:c.19-49T>C	NP_006507.2:n.19-49T>C
NM_006516.4:c.19-49T>C MANE Select	NP_006507.2:n.19-49T>C