Canonical Allele Identifier: CA735975281

Gene: SLC2A1

Linked Data

• dbSNP Id: rs1439513832
• gnomAD v3: 1-42936992-C-T
• gnomAD v4: 1-42936992-C-T
• MyVariant Identifiers: chr1:g.43402663C>T (hg19) ; chr1:g.42936992C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42936992C>T , CM000663.2:g.42936992C>T	GRCh38
NC_000001.10:g.43402663C>T , CM000663.1:g.43402663C>T	GRCh37
NC_000001.9:g.43175250C>T	NCBI36
NG_008232.1:g.27185G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.115-5786G>A MANE Select	ENSP00000416293.2:n.115-5786G>A
ENST00000674765.1:c.115-5786G>A	ENSP00000501811.1:n.115-5786G>A
ENST00000675112.1:n.138-5786G>A
ENST00000372500.4:c.19-5786G>A	ENSP00000361578.4:n.19-5786G>A
ENST00000415851.6:n.332-5786G>A
ENST00000426263.7:c.115-5786G>A	ENSP00000416293.2:n.115-5786G>A
ENST00000475162.3:c.14-5786G>A
ENST00000625233.2:n.323-5786G>A
ENST00000628173.1:n.460+2831G>A
ENST00000630287.2:c.115-5786G>A	ENSP00000486694.1:n.115-5786G>A
NM_006516.2:c.115-5786G>A	NP_006507.2:n.115-5786G>A
NM_006516.3:c.115-5786G>A	NP_006507.2:n.115-5786G>A
NM_006516.4:c.115-5786G>A MANE Select	NP_006507.2:n.115-5786G>A