Canonical Allele Identifier: CA1141188966
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929751C= , CM000663.2:g.42929751C= GRCh38
NC_000001.10:g.43395422C= , CM000663.1:g.43395422C= GRCh37
NC_000001.9:g.43168009C= NCBI36
NG_008232.1:g.34426G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.709G= MANE Select ENSP00000416293.2:p.Val237=
ENST00000669445.1:c.57-18G=
ENST00000674765.1:c.709G= ENSP00000501811.1:p.Val237=
ENST00000675112.1:n.732G=
ENST00000676254.1:n.1158G=
ENST00000426263.7:c.709G= ENSP00000416293.2:p.Val237=
ENST00000439722.2:c.588G= ENSP00000395521.2:n.588G=
ENST00000475162.3:c.415+875G=
ENST00000630287.2:c.*24G= ENSP00000486694.1:n.*24G=
NM_006516.2:c.709G= NP_006507.2:p.Val237=
NM_006516.3:c.709G= NP_006507.2:p.Val237=
NM_006516.4:c.709G= MANE Select NP_006507.2:p.Val237=