Canonical Allele Identifier: CA1165412297
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929513C= , CM000663.2:g.42929513C= GRCh38
NC_000001.10:g.43395184C= , CM000663.1:g.43395184C= GRCh37
NC_000001.9:g.43167771C= NCBI36
NG_008232.1:g.34664G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.867+80G= MANE Select ENSP00000416293.2:n.867+80G=
ENST00000674765.1:c.867+80G= ENSP00000501811.1:n.867+80G=
ENST00000675112.1:n.970G=
ENST00000676254.1:n.1316+80G=
ENST00000426263.7:c.867+80G= ENSP00000416293.2:n.867+80G=
ENST00000439722.2:c.746+80G= ENSP00000395521.2:n.746+80G=
ENST00000475162.3:c.415+1113G=
ENST00000630287.2:c.*182+80G= ENSP00000486694.1:n.*182+80G=
NM_006516.2:c.867+80G= NP_006507.2:n.867+80G=
NM_006516.3:c.867+80G= NP_006507.2:n.867+80G=
NM_006516.4:c.867+80G= MANE Select NP_006507.2:n.867+80G=