Canonical Allele Identifier: CA2695703707
Gene: SLC2A1 HGNC NCBI

Linked Data

dbSNP Id: rs2124456267

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42936973C>T , CM000663.2:g.42936973C>T GRCh38
NC_000001.10:g.43402644C>T , CM000663.1:g.43402644C>T GRCh37
NC_000001.9:g.43175231C>T NCBI36
NG_008232.1:g.27204G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000426263.10:c.115-5767G>A MANE Select ENSP00000416293.2:n.115-5767G>A
ENST00000674765.1:c.115-5767G>A ENSP00000501811.1:n.115-5767G>A
ENST00000675112.1:n.138-5767G>A
ENST00000372500.4:c.19-5767G>A ENSP00000361578.4:n.19-5767G>A
ENST00000415851.6:n.332-5767G>A
ENST00000426263.7:c.115-5767G>A ENSP00000416293.2:n.115-5767G>A
ENST00000475162.3:c.14-5767G>A
ENST00000625233.2:n.323-5767G>A
ENST00000628173.1:n.460+2850G>A
ENST00000630287.2:c.115-5767G>A ENSP00000486694.1:n.115-5767G>A
NM_006516.2:c.115-5767G>A NP_006507.2:n.115-5767G>A
NM_006516.3:c.115-5767G>A NP_006507.2:n.115-5767G>A
NM_006516.4:c.115-5767G>A MANE Select NP_006507.2:n.115-5767G>A