Canonical Allele Identifier: CA1141580740
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929242C= , CM000663.2:g.42929242C= GRCh38
NC_000001.10:g.43394913C= , CM000663.1:g.43394913C= GRCh37
NC_000001.9:g.43167500C= NCBI36
NG_008232.1:g.34935G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.940G= MANE Select ENSP00000416293.2:p.Gly314=
ENST00000674545.1:n.258G=
ENST00000674765.1:c.940G= ENSP00000501811.1:p.Gly314=
ENST00000675112.1:n.1241G=
ENST00000676254.1:n.1389G=
ENST00000426263.7:c.940G= ENSP00000416293.2:p.Gly314=
ENST00000439722.2:c.819G= ENSP00000395521.2:n.819G=
ENST00000475162.3:c.415+1384G=
ENST00000630287.2:c.*255G= ENSP00000486694.1:n.*255G=
NM_006516.2:c.940G= NP_006507.2:p.Gly314=
NM_006516.3:c.940G= NP_006507.2:p.Gly314=
NM_006516.4:c.940G= MANE Select NP_006507.2:p.Gly314=