Canonical Allele Identifier: CA2670005222

Gene: SLC2A9

Linked Data

• gnomAD v4: 4-10034865-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.10034865C>A , CM000666.2:g.10034865C>A	GRCh38
NC_000004.11:g.10036489C>A , CM000666.1:g.10036489C>A	GRCh37
NC_000004.10:g.9645587C>A	NCBI36
NG_011540.1:g.10384G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309065.7:c.-41+5265G>T	ENSP00000311383.3:n.-41+5265G>T
ENST00000481042.1:n.1535G>T
ENST00000505104.5:n.81+5265G>T
ENST00000506583.5:c.-41+5265G>T	ENSP00000422209.1:n.-41+5265G>T
ENST00000513129.1:c.-40-8859G>T	ENSP00000426800.1:n.-40-8859G>T
NM_001001290.1:c.-41+5265G>T	NP_001001290.1:n.-41+5265G>T
XM_006713969.2:c.-41+5265G>T	XP_006714032.1:n.-41+5265G>T
XM_011513857.1:c.-41+5265G>T	XP_011512159.1:n.-41+5265G>T
NM_001001290.2:c.-41+5265G>T	NP_001001290.1:n.-41+5265G>T