Canonical Allele Identifier: CA784341298

Gene: SLC2A9

Linked Data

• dbSNP Id: rs1458397766
• gnomAD v3: 4-10034833-AAAG-A
• gnomAD v4: 4-10034833-AAAG-A
• MyVariant Identifiers: chr4:g.10036458_10036460del (hg19) ; chr4:g.10034834_10034836del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.10034837_10034839del , CM000666.2:g.10034837_10034839del	GRCh38
NC_000004.11:g.10036461_10036463del , CM000666.1:g.10036461_10036463del	GRCh37
NC_000004.10:g.9645559_9645561del	NCBI36
NG_011540.1:g.10413_10415del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309065.7:c.-41+5294_-41+5296del	ENSP00000311383.3:n.-41+5294_-41+5296del
ENST00000481042.1:n.1564_1566del
ENST00000505104.5:n.81+5294_81+5296del
ENST00000506583.5:c.-41+5294_-41+5296del	ENSP00000422209.1:n.-41+5294_-41+5296del
ENST00000513129.1:c.-40-8830_-40-8828del	ENSP00000426800.1:n.-40-8830_-40-8828del
NM_001001290.1:c.-41+5294_-41+5296del	NP_001001290.1:n.-41+5294_-41+5296del
XM_006713969.2:c.-41+5294_-41+5296del	XP_006714032.1:n.-41+5294_-41+5296del
XM_011513857.1:c.-41+5294_-41+5296del	XP_011512159.1:n.-41+5294_-41+5296del
NM_001001290.2:c.-41+5294_-41+5296del	NP_001001290.1:n.-41+5294_-41+5296del