Canonical Allele Identifier: CA1437812266

Gene: SLC2A9

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.10034963_10034964delinsCT , CM000666.2:g.10034963_10034964delinsCT	GRCh38
NC_000004.11:g.10036587_10036588delinsCT , CM000666.1:g.10036587_10036588delinsCT	GRCh37
NC_000004.10:g.9645685_9645686delinsCT	NCBI36
NG_011540.1:g.10285_10286delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309065.7:c.-41+5166_-41+5167delinsAG	ENSP00000311383.3:n.-41+5166_-41+5167delinsAG
ENST00000481042.1:n.1436_1437delinsAG
ENST00000505104.5:n.81+5166_81+5167delinsAG
ENST00000506583.5:c.-41+5166_-41+5167delinsAG	ENSP00000422209.1:n.-41+5166_-41+5167delinsAG
ENST00000513129.1:c.-40-8958_-40-8957delinsAG	ENSP00000426800.1:n.-40-8958_-40-8957delinsAG
NM_001001290.1:c.-41+5166_-41+5167delinsAG	NP_001001290.1:n.-41+5166_-41+5167delinsAG
XM_006713969.2:c.-41+5166_-41+5167delinsAG	XP_006714032.1:n.-41+5166_-41+5167delinsAG
XM_011513857.1:c.-41+5166_-41+5167delinsAG	XP_011512159.1:n.-41+5166_-41+5167delinsAG
NM_001001290.2:c.-41+5166_-41+5167delinsAG	NP_001001290.1:n.-41+5166_-41+5167delinsAG