Canonical Allele Identifier: CA1165412760
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930686A= , CM000663.2:g.42930686A= GRCh38
NC_000001.10:g.43396357A= , CM000663.1:g.43396357A= GRCh37
NC_000001.9:g.43168944A= NCBI36
NG_008232.1:g.33491T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.456T= MANE Select ENSP00000416293.2:p.Leu152=
ENST00000674765.1:c.456T= ENSP00000501811.1:p.Leu152=
ENST00000675112.1:n.479T=
ENST00000676254.1:n.905T=
ENST00000426263.7:c.456T= ENSP00000416293.2:p.Leu152=
ENST00000439722.2:c.335T= ENSP00000395521.2:n.335T=
ENST00000475162.3:c.355T=
ENST00000625233.2:n.664T=
ENST00000630287.2:c.456T= ENSP00000486694.1:p.Leu152=
NM_006516.2:c.456T= NP_006507.2:p.Leu152=
NM_006516.3:c.456T= NP_006507.2:p.Leu152=
NM_006516.4:c.456T= MANE Select NP_006507.2:p.Leu152=