Canonical Allele Identifier: CA1165412431
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929880G= , CM000663.2:g.42929880G= GRCh38
NC_000001.10:g.43395551G= , CM000663.1:g.43395551G= GRCh37
NC_000001.9:g.43168138G= NCBI36
NG_008232.1:g.34297C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.672C= MANE Select ENSP00000416293.2:p.Ala224=
ENST00000669445.1:c.49C=
ENST00000674765.1:c.672C= ENSP00000501811.1:p.Ala224=
ENST00000675112.1:n.695C=
ENST00000676254.1:n.1121C=
ENST00000426263.7:c.672C= ENSP00000416293.2:p.Ala224=
ENST00000439722.2:c.551C= ENSP00000395521.2:n.551C=
ENST00000475162.3:c.415+746C=
ENST00000630287.2:c.517-100C= ENSP00000486694.1:n.517-100C=
NM_006516.2:c.672C= NP_006507.2:p.Ala224=
NM_006516.3:c.672C= NP_006507.2:p.Ala224=
NM_006516.4:c.672C= MANE Select NP_006507.2:p.Ala224=