Canonical Allele Identifier: CA1141188970
Community Standard Title: NM_006516.4(SLC2A1):c.18+1G=
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42958633C= , CM000663.2:g.42958633C= GRCh38
NC_000001.10:g.43424304C= , CM000663.1:g.43424304C= GRCh37
NC_000001.9:g.43196891C= NCBI36
NG_008232.1:g.5544G=

Transcript Alleles

HGVS Amino-acid Change
NM_006516.4:c.18+1G= MANE Select NP_006507.2:n.18+1G=
ENST00000426263.10:c.18+1G= MANE Select ENSP00000416293.2:n.18+1G=
NM_006516.2:c.18+1G= NP_006507.2:n.18+1G=
NM_006516.3:c.18+1G= NP_006507.2:n.18+1G=
ENST00000372500.4:c.18+1G= ENSP00000361578.4:n.18+1G=
ENST00000415851.6:n.235+1G=
ENST00000426263.7:c.18+1G= ENSP00000416293.2:n.18+1G=
ENST00000460369.2:n.226+1G=
ENST00000460369.3:c.18+1G= ENSP00000491942.1:n.18+1G=
ENST00000625233.2:n.226+1G=
ENST00000628173.1:n.237+1G=
ENST00000630287.2:c.18+1G= ENSP00000486694.1:n.18+1G=
ENST00000630821.1:n.235+1G=
ENST00000674765.1:c.18+1G= ENSP00000501811.1:n.18+1G=
ENST00000675112.1:n.41+1G=
ENST00000676097.1:n.260+1G=