Canonical Allele Identifier: CA1165412321
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929567C= , CM000663.2:g.42929567C= GRCh38
NC_000001.10:g.43395238C= , CM000663.1:g.43395238C= GRCh37
NC_000001.9:g.43167825C= NCBI36
NG_008232.1:g.34610G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.867+26G= MANE Select ENSP00000416293.2:n.867+26G=
ENST00000674765.1:c.867+26G= ENSP00000501811.1:n.867+26G=
ENST00000675112.1:n.916G=
ENST00000676254.1:n.1316+26G=
ENST00000426263.7:c.867+26G= ENSP00000416293.2:n.867+26G=
ENST00000439722.2:c.746+26G= ENSP00000395521.2:n.746+26G=
ENST00000475162.3:c.415+1059G=
ENST00000630287.2:c.*182+26G= ENSP00000486694.1:n.*182+26G=
NM_006516.2:c.867+26G= NP_006507.2:n.867+26G=
NM_006516.3:c.867+26G= NP_006507.2:n.867+26G=
NM_006516.4:c.867+26G= MANE Select NP_006507.2:n.867+26G=