Canonical Allele Identifier: CA1165417707
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42943077T= , CM000663.2:g.42943077T= GRCh38
NC_000001.10:g.43408748T= , CM000663.1:g.43408748T= GRCh37
NC_000001.9:g.43181335T= NCBI36
NG_008232.1:g.21100A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.114+149A= MANE Select ENSP00000416293.2:n.114+149A=
ENST00000674765.1:c.114+149A= ENSP00000501811.1:n.114+149A=
ENST00000675112.1:n.137+149A=
ENST00000372500.4:c.19-11871A= ENSP00000361578.4:n.19-11871A=
ENST00000415851.6:n.331+149A=
ENST00000426263.7:c.114+149A= ENSP00000416293.2:n.114+149A=
ENST00000475162.3:c.13+149A=
ENST00000625233.2:n.322+149A=
ENST00000628173.1:n.333+149A=
ENST00000630287.2:c.114+149A= ENSP00000486694.1:n.114+149A=
ENST00000630821.1:n.480A=
NM_006516.2:c.114+149A= NP_006507.2:n.114+149A=
NM_006516.3:c.114+149A= NP_006507.2:n.114+149A=
NM_006516.4:c.114+149A= MANE Select NP_006507.2:n.114+149A=