Canonical Allele Identifier: CA1165412444
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929921G= , CM000663.2:g.42929921G= GRCh38
NC_000001.10:g.43395592G= , CM000663.1:g.43395592G= GRCh37
NC_000001.9:g.43168179G= NCBI36
NG_008232.1:g.34256C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.631C= MANE Select ENSP00000416293.2:p.Pro211=
ENST00000669445.1:c.8C=
ENST00000674765.1:c.631C= ENSP00000501811.1:p.Pro211=
ENST00000675112.1:n.654C=
ENST00000676254.1:n.1080C=
ENST00000426263.7:c.631C= ENSP00000416293.2:p.Pro211=
ENST00000439722.2:c.510C= ENSP00000395521.2:n.510C=
ENST00000475162.3:c.415+705C=
ENST00000630287.2:c.517-141C= ENSP00000486694.1:n.517-141C=
NM_006516.2:c.631C= NP_006507.2:p.Pro211=
NM_006516.3:c.631C= NP_006507.2:p.Pro211=
NM_006516.4:c.631C= MANE Select NP_006507.2:p.Pro211=