Canonical Allele Identifier: CA1165417895
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42943563T= , CM000663.2:g.42943563T= GRCh38
NC_000001.10:g.43409234T= , CM000663.1:g.43409234T= GRCh37
NC_000001.9:g.43181821T= NCBI36
NG_008232.1:g.20614A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.19-242A= MANE Select ENSP00000416293.2:n.19-242A=
ENST00000674765.1:c.19-242A= ENSP00000501811.1:n.19-242A=
ENST00000675112.1:n.42-242A=
ENST00000372500.4:c.19-12357A= ENSP00000361578.4:n.19-12357A=
ENST00000415851.6:n.236-242A=
ENST00000426263.7:c.19-242A= ENSP00000416293.2:n.19-242A=
ENST00000625233.2:n.227-242A=
ENST00000628173.1:n.238-242A=
ENST00000630287.2:c.19-242A= ENSP00000486694.1:n.19-242A=
ENST00000630821.1:n.236-242A=
NM_006516.2:c.19-242A= NP_006507.2:n.19-242A=
NM_006516.3:c.19-242A= NP_006507.2:n.19-242A=
NM_006516.4:c.19-242A= MANE Select NP_006507.2:n.19-242A=