Canonical Allele Identifier: CA1148719598
Gene: SLC2A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42943511A= , CM000663.2:g.42943511A= GRCh38
NC_000001.10:g.43409182A= , CM000663.1:g.43409182A= GRCh37
NC_000001.9:g.43181769A= NCBI36
NG_008232.1:g.20666T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.19-190T= MANE Select ENSP00000416293.2:n.19-190T=
ENST00000674765.1:c.19-190T= ENSP00000501811.1:n.19-190T=
ENST00000675112.1:n.42-190T=
ENST00000372500.4:c.19-12305T= ENSP00000361578.4:n.19-12305T=
ENST00000415851.6:n.236-190T=
ENST00000426263.7:c.19-190T= ENSP00000416293.2:n.19-190T=
ENST00000625233.2:n.227-190T=
ENST00000628173.1:n.238-190T=
ENST00000630287.2:c.19-190T= ENSP00000486694.1:n.19-190T=
ENST00000630821.1:n.236-190T=
NM_006516.2:c.19-190T= NP_006507.2:n.19-190T=
NM_006516.3:c.19-190T= NP_006507.2:n.19-190T=
NM_006516.4:c.19-190T= MANE Select NP_006507.2:n.19-190T=
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