Canonical Allele Identifier: CA1437812297
Gene: SLC2A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.10035025C= , CM000666.2:g.10035025C= GRCh38
NC_000004.11:g.10036649C= , CM000666.1:g.10036649C= GRCh37
NC_000004.10:g.9645747C= NCBI36
NG_011540.1:g.10224G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309065.7:c.-41+5105G= ENSP00000311383.3:n.-41+5105G=
ENST00000481042.1:n.1375G=
ENST00000505104.5:n.81+5105G=
ENST00000506583.5:c.-41+5105G= ENSP00000422209.1:n.-41+5105G=
ENST00000513129.1:c.-40-9019G= ENSP00000426800.1:n.-40-9019G=
NM_001001290.1:c.-41+5105G= NP_001001290.1:n.-41+5105G=
XM_006713969.2:c.-41+5105G= XP_006714032.1:n.-41+5105G=
XM_011513857.1:c.-41+5105G= XP_011512159.1:n.-41+5105G=
NM_001001290.2:c.-41+5105G= NP_001001290.1:n.-41+5105G=