Canonical Allele Identifier: CA1165415280
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42936992C= , CM000663.2:g.42936992C= GRCh38
NC_000001.10:g.43402663C= , CM000663.1:g.43402663C= GRCh37
NC_000001.9:g.43175250C= NCBI36
NG_008232.1:g.27185G=

Transcript Alleles

HGVS Amino-acid change
ENST00000426263.10:c.115-5786G= MANE Select ENSP00000416293.2:n.115-5786G=
ENST00000674765.1:c.115-5786G= ENSP00000501811.1:n.115-5786G=
ENST00000675112.1:n.138-5786G=
ENST00000372500.4:c.19-5786G= ENSP00000361578.4:n.19-5786G=
ENST00000415851.6:n.332-5786G=
ENST00000426263.7:c.115-5786G= ENSP00000416293.2:n.115-5786G=
ENST00000475162.3:c.14-5786G=
ENST00000625233.2:n.323-5786G=
ENST00000628173.1:n.460+2831G=
ENST00000630287.2:c.115-5786G= ENSP00000486694.1:n.115-5786G=
NM_006516.2:c.115-5786G= NP_006507.2:n.115-5786G=
NM_006516.3:c.115-5786G= NP_006507.2:n.115-5786G=
NM_006516.4:c.115-5786G= MANE Select NP_006507.2:n.115-5786G=