Canonical Allele Identifier: CA1141617479
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42927722T= , CM000663.2:g.42927722T= GRCh38
NC_000001.10:g.43393393T= , CM000663.1:g.43393393T= GRCh37
NC_000001.9:g.43165980T= NCBI36
NG_008232.1:g.36455A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.1161A= MANE Select ENSP00000416293.2:p.Pro387=
ENST00000674545.1:n.1778A=
ENST00000674765.1:c.1030-865A= ENSP00000501811.1:n.1030-865A=
ENST00000675112.1:n.1462A=
ENST00000676254.1:n.1610A=
ENST00000426263.7:c.1161A= ENSP00000416293.2:p.Pro387=
ENST00000475162.3:c.416-744A=
ENST00000630287.2:c.*476A= ENSP00000486694.1:n.*476A=
NM_006516.2:c.1161A= NP_006507.2:p.Pro387=
NM_006516.3:c.1161A= NP_006507.2:p.Pro387=
NM_006516.4:c.1161A= MANE Select NP_006507.2:p.Pro387=