Canonical Allele Identifier: CA1437812136
Gene: SLC2A9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.10034638A= , CM000666.2:g.10034638A= GRCh38
NC_000004.11:g.10036262A= , CM000666.1:g.10036262A= GRCh37
NC_000004.10:g.9645360A= NCBI36
NG_011540.1:g.10611T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309065.7:c.-41+5492T= ENSP00000311383.3:n.-41+5492T=
ENST00000481042.1:n.1762T=
ENST00000505104.5:n.81+5492T=
ENST00000506583.5:c.-41+5492T= ENSP00000422209.1:n.-41+5492T=
ENST00000513129.1:c.-40-8632T= ENSP00000426800.1:n.-40-8632T=
NM_001001290.1:c.-41+5492T= NP_001001290.1:n.-41+5492T=
XM_006713969.2:c.-41+5492T= XP_006714032.1:n.-41+5492T=
XM_011513857.1:c.-41+5492T= XP_011512159.1:n.-41+5492T=
NM_001001290.2:c.-41+5492T= NP_001001290.1:n.-41+5492T=
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