Canonical Allele Identifier: CA1165417858
Gene: SLC2A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42943460T= , CM000663.2:g.42943460T= GRCh38
NC_000001.10:g.43409131T= , CM000663.1:g.43409131T= GRCh37
NC_000001.9:g.43181718T= NCBI36
NG_008232.1:g.20717A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.19-139A= MANE Select ENSP00000416293.2:n.19-139A=
ENST00000674765.1:c.19-139A= ENSP00000501811.1:n.19-139A=
ENST00000675112.1:n.42-139A=
ENST00000372500.4:c.19-12254A= ENSP00000361578.4:n.19-12254A=
ENST00000415851.6:n.236-139A=
ENST00000426263.7:c.19-139A= ENSP00000416293.2:n.19-139A=
ENST00000625233.2:n.227-139A=
ENST00000628173.1:n.238-139A=
ENST00000630287.2:c.19-139A= ENSP00000486694.1:n.19-139A=
ENST00000630821.1:n.236-139A=
NM_006516.2:c.19-139A= NP_006507.2:n.19-139A=
NM_006516.3:c.19-139A= NP_006507.2:n.19-139A=
NM_006516.4:c.19-139A= MANE Select NP_006507.2:n.19-139A=
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