Canonical Allele Identifier: CA1165412612
Gene: SLC2A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930347G= , CM000663.2:g.42930347G= GRCh38
NC_000001.10:g.43396018G= , CM000663.1:g.43396018G= GRCh37
NC_000001.9:g.43168605G= NCBI36
NG_008232.1:g.33830C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.516+279C= MANE Select ENSP00000416293.2:n.516+279C=
ENST00000674765.1:c.516+279C= ENSP00000501811.1:n.516+279C=
ENST00000675112.1:n.539+279C=
ENST00000676254.1:n.965+279C=
ENST00000426263.7:c.516+279C= ENSP00000416293.2:n.516+279C=
ENST00000439722.2:c.395+279C= ENSP00000395521.2:n.395+279C=
ENST00000475162.3:c.415+279C=
ENST00000625233.2:n.1003C=
ENST00000630287.2:c.516+279C= ENSP00000486694.1:n.516+279C=
NM_006516.2:c.516+279C= NP_006507.2:n.516+279C=
NM_006516.3:c.516+279C= NP_006507.2:n.516+279C=
NM_006516.4:c.516+279C= MANE Select NP_006507.2:n.516+279C=
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