Canonical Allele Identifier: CA735977835

Gene: SLC2A1

Linked Data

• dbSNP Id: rs1304607175
• gnomAD v3: 1-42943111-T-G
• gnomAD v4: 1-42943111-T-G
• MyVariant Identifiers: chr1:g.43408782T>G (hg19) ; chr1:g.42943111T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42943111T>G , CM000663.2:g.42943111T>G	GRCh38
NC_000001.10:g.43408782T>G , CM000663.1:g.43408782T>G	GRCh37
NC_000001.9:g.43181369T>G	NCBI36
NG_008232.1:g.21066A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.114+115A>C MANE Select	ENSP00000416293.2:n.114+115A>C
ENST00000674765.1:c.114+115A>C	ENSP00000501811.1:n.114+115A>C
ENST00000675112.1:n.137+115A>C
ENST00000372500.4:c.19-11905A>C	ENSP00000361578.4:n.19-11905A>C
ENST00000415851.6:n.331+115A>C
ENST00000426263.7:c.114+115A>C	ENSP00000416293.2:n.114+115A>C
ENST00000475162.3:c.13+115A>C
ENST00000625233.2:n.322+115A>C
ENST00000628173.1:n.333+115A>C
ENST00000630287.2:c.114+115A>C	ENSP00000486694.1:n.114+115A>C
ENST00000630821.1:n.446A>C
NM_006516.2:c.114+115A>C	NP_006507.2:n.114+115A>C
NM_006516.3:c.114+115A>C	NP_006507.2:n.114+115A>C
NM_006516.4:c.114+115A>C MANE Select	NP_006507.2:n.114+115A>C