Canonical Allele Identifier: CA1140438791
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929866C= , CM000663.2:g.42929866C= GRCh38
NC_000001.10:g.43395537C= , CM000663.1:g.43395537C= GRCh37
NC_000001.9:g.43168124C= NCBI36
NG_008232.1:g.34311G=

Transcript Alleles

HGVS Amino-acid change
ENST00000426263.10:c.679+7G= MANE Select ENSP00000416293.2:n.679+7G=
ENST00000669445.1:c.56+7G=
ENST00000674765.1:c.679+7G= ENSP00000501811.1:n.679+7G=
ENST00000675112.1:n.702+7G=
ENST00000676254.1:n.1128+7G=
ENST00000426263.7:c.679+7G= ENSP00000416293.2:n.679+7G=
ENST00000439722.2:c.558+7G= ENSP00000395521.2:n.558+7G=
ENST00000475162.3:c.415+760G=
ENST00000630287.2:c.517-86G= ENSP00000486694.1:n.517-86G=
NM_006516.2:c.679+7G= NP_006507.2:n.679+7G=
NM_006516.3:c.679+7G= NP_006507.2:n.679+7G=
NM_006516.4:c.679+7G= MANE Select NP_006507.2:n.679+7G=