Canonical Allele Identifier: CA1145166993
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930799G= , CM000663.2:g.42930799G= GRCh38
NC_000001.10:g.43396470G= , CM000663.1:g.43396470G= GRCh37
NC_000001.9:g.43169057G= NCBI36
NG_008232.1:g.33378C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.343C= MANE Select ENSP00000416293.2:p.Leu115=
ENST00000674765.1:c.343C= ENSP00000501811.1:p.Leu115=
ENST00000675112.1:n.366C=
ENST00000676254.1:n.792C=
ENST00000372500.4:c.247C= ENSP00000361578.4:p.Leu83=
ENST00000426263.7:c.343C= ENSP00000416293.2:p.Leu115=
ENST00000439722.2:c.222C= ENSP00000395521.2:n.222C=
ENST00000475162.3:c.242C=
ENST00000625233.2:n.551C=
ENST00000630287.2:c.343C= ENSP00000486694.1:p.Leu115=
NM_006516.2:c.343C= NP_006507.2:p.Leu115=
NM_006516.3:c.343C= NP_006507.2:p.Leu115=
NM_006516.4:c.343C= MANE Select NP_006507.2:p.Leu115=