Canonical Allele Identifier: CA1147406343
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929829C= , CM000663.2:g.42929829C= GRCh38
NC_000001.10:g.43395500C= , CM000663.1:g.43395500C= GRCh37
NC_000001.9:g.43168087C= NCBI36
NG_008232.1:g.34348G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.679+44G= MANE Select ENSP00000416293.2:n.679+44G=
ENST00000669445.1:c.56+44G=
ENST00000674765.1:c.679+44G= ENSP00000501811.1:n.679+44G=
ENST00000675112.1:n.702+44G=
ENST00000676254.1:n.1128+44G=
ENST00000426263.7:c.679+44G= ENSP00000416293.2:n.679+44G=
ENST00000439722.2:c.558+44G= ENSP00000395521.2:n.558+44G=
ENST00000475162.3:c.415+797G=
ENST00000630287.2:c.517-49G= ENSP00000486694.1:n.517-49G=
NM_006516.2:c.679+44G= NP_006507.2:n.679+44G=
NM_006516.3:c.679+44G= NP_006507.2:n.679+44G=
NM_006516.4:c.679+44G= MANE Select NP_006507.2:n.679+44G=