Canonical Allele Identifier: CA2670005151

Gene: SLC2A9

Linked Data

• gnomAD v4: 4-10034740-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.10034740T>C , CM000666.2:g.10034740T>C	GRCh38
NC_000004.11:g.10036364T>C , CM000666.1:g.10036364T>C	GRCh37
NC_000004.10:g.9645462T>C	NCBI36
NG_011540.1:g.10509A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000309065.7:c.-41+5390A>G	ENSP00000311383.3:n.-41+5390A>G
ENST00000481042.1:n.1660A>G
ENST00000505104.5:n.81+5390A>G
ENST00000506583.5:c.-41+5390A>G	ENSP00000422209.1:n.-41+5390A>G
ENST00000513129.1:c.-40-8734A>G	ENSP00000426800.1:n.-40-8734A>G
NM_001001290.1:c.-41+5390A>G	NP_001001290.1:n.-41+5390A>G
XM_006713969.2:c.-41+5390A>G	XP_006714032.1:n.-41+5390A>G
XM_011513857.1:c.-41+5390A>G	XP_011512159.1:n.-41+5390A>G
NM_001001290.2:c.-41+5390A>G	NP_001001290.1:n.-41+5390A>G