Canonical Allele Identifier: CA1165417877
Gene: SLC2A1 HGNC NCBI

Linked Data

dbSNP Id: rs1643619727

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42943533C>G , CM000663.2:g.42943533C>G GRCh38
NC_000001.10:g.43409204C>G , CM000663.1:g.43409204C>G GRCh37
NC_000001.9:g.43181791C>G NCBI36
NG_008232.1:g.20644G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.19-212G>C MANE Select ENSP00000416293.2:n.19-212G>C
ENST00000674765.1:c.19-212G>C ENSP00000501811.1:n.19-212G>C
ENST00000675112.1:n.42-212G>C
ENST00000372500.4:c.19-12327G>C ENSP00000361578.4:n.19-12327G>C
ENST00000415851.6:n.236-212G>C
ENST00000426263.7:c.19-212G>C ENSP00000416293.2:n.19-212G>C
ENST00000625233.2:n.227-212G>C
ENST00000628173.1:n.238-212G>C
ENST00000630287.2:c.19-212G>C ENSP00000486694.1:n.19-212G>C
ENST00000630821.1:n.236-212G>C
NM_006516.2:c.19-212G>C NP_006507.2:n.19-212G>C
NM_006516.3:c.19-212G>C NP_006507.2:n.19-212G>C
NM_006516.4:c.19-212G>C MANE Select NP_006507.2:n.19-212G>C