Canonical Allele Identifier: CA1144228775
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929884C= , CM000663.2:g.42929884C= GRCh38
NC_000001.10:g.43395555C= , CM000663.1:g.43395555C= GRCh37
NC_000001.9:g.43168142C= NCBI36
NG_008232.1:g.34293G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.668G= MANE Select ENSP00000416293.2:p.Arg223=
ENST00000669445.1:c.45G=
ENST00000674765.1:c.668G= ENSP00000501811.1:p.Arg223=
ENST00000675112.1:n.691G=
ENST00000676254.1:n.1117G=
ENST00000426263.7:c.668G= ENSP00000416293.2:p.Arg223=
ENST00000439722.2:c.547G= ENSP00000395521.2:n.547G=
ENST00000475162.3:c.415+742G=
ENST00000630287.2:c.517-104G= ENSP00000486694.1:n.517-104G=
NM_006516.2:c.668G= NP_006507.2:p.Arg223=
NM_006516.3:c.668G= NP_006507.2:p.Arg223=
NM_006516.4:c.668G= MANE Select NP_006507.2:p.Arg223=