Canonical Allele Identifier: CA1165412185
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929245A= , CM000663.2:g.42929245A= GRCh38
NC_000001.10:g.43394916A= , CM000663.1:g.43394916A= GRCh37
NC_000001.9:g.43167503A= NCBI36
NG_008232.1:g.34932T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.937T= MANE Select ENSP00000416293.2:p.Ser313=
ENST00000674545.1:n.255T=
ENST00000674765.1:c.937T= ENSP00000501811.1:p.Ser313=
ENST00000675112.1:n.1238T=
ENST00000676254.1:n.1386T=
ENST00000426263.7:c.937T= ENSP00000416293.2:p.Ser313=
ENST00000439722.2:c.816T= ENSP00000395521.2:n.816T=
ENST00000475162.3:c.415+1381T=
ENST00000630287.2:c.*252T= ENSP00000486694.1:n.*252T=
NM_006516.2:c.937T= NP_006507.2:p.Ser313=
NM_006516.3:c.937T= NP_006507.2:p.Ser313=
NM_006516.4:c.937T= MANE Select NP_006507.2:p.Ser313=