Canonical Allele Identifier: CA2760399058
Gene: SLC2A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.10034913T>A , CM000666.2:g.10034913T>A GRCh38
NC_000004.11:g.10036537T>A , CM000666.1:g.10036537T>A GRCh37
NC_000004.10:g.9645635T>A NCBI36
NG_011540.1:g.10336A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309065.7:c.-41+5217A>T ENSP00000311383.3:n.-41+5217A>T
ENST00000481042.1:n.1487A>T
ENST00000505104.5:n.81+5217A>T
ENST00000506583.5:c.-41+5217A>T ENSP00000422209.1:n.-41+5217A>T
ENST00000513129.1:c.-40-8907A>T ENSP00000426800.1:n.-40-8907A>T
NM_001001290.1:c.-41+5217A>T NP_001001290.1:n.-41+5217A>T
XM_006713969.2:c.-41+5217A>T XP_006714032.1:n.-41+5217A>T
XM_011513857.1:c.-41+5217A>T XP_011512159.1:n.-41+5217A>T
NM_001001290.2:c.-41+5217A>T NP_001001290.1:n.-41+5217A>T