Canonical Allele Identifier: CA1165417750
Gene: SLC2A1 HGNC NCBI

Linked Data

dbSNP Id: rs770483506

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42943194T>G , CM000663.2:g.42943194T>G GRCh38
NC_000001.10:g.43408865T>G , CM000663.1:g.43408865T>G GRCh37
NC_000001.9:g.43181452T>G NCBI36
NG_008232.1:g.20983A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.114+32A>C MANE Select ENSP00000416293.2:n.114+32A>C
ENST00000674765.1:c.114+32A>C ENSP00000501811.1:n.114+32A>C
ENST00000675112.1:n.137+32A>C
ENST00000372500.4:c.19-11988A>C ENSP00000361578.4:n.19-11988A>C
ENST00000415851.6:n.331+32A>C
ENST00000426263.7:c.114+32A>C ENSP00000416293.2:n.114+32A>C
ENST00000475162.3:c.13+32A>C
ENST00000625233.2:n.322+32A>C
ENST00000628173.1:n.333+32A>C
ENST00000630287.2:c.114+32A>C ENSP00000486694.1:n.114+32A>C
ENST00000630821.1:n.363A>C
NM_006516.2:c.114+32A>C NP_006507.2:n.114+32A>C
NM_006516.3:c.114+32A>C NP_006507.2:n.114+32A>C
NM_006516.4:c.114+32A>C MANE Select NP_006507.2:n.114+32A>C