Canonical Allele Identifier: CA1165412769
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930718T= , CM000663.2:g.42930718T= GRCh38
NC_000001.10:g.43396389T= , CM000663.1:g.43396389T= GRCh37
NC_000001.9:g.43168976T= NCBI36
NG_008232.1:g.33459A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.424A= MANE Select ENSP00000416293.2:p.Met142=
ENST00000674765.1:c.424A= ENSP00000501811.1:p.Met142=
ENST00000675112.1:n.447A=
ENST00000676254.1:n.873A=
ENST00000372500.4:c.328A= ENSP00000361578.4:p.Met110=
ENST00000426263.7:c.424A= ENSP00000416293.2:p.Met142=
ENST00000439722.2:c.303A= ENSP00000395521.2:n.303A=
ENST00000475162.3:c.323A=
ENST00000625233.2:n.632A=
ENST00000630287.2:c.424A= ENSP00000486694.1:p.Met142=
NM_006516.2:c.424A= NP_006507.2:p.Met142=
NM_006516.3:c.424A= NP_006507.2:p.Met142=
NM_006516.4:c.424A= MANE Select NP_006507.2:p.Met142=