Canonical Allele Identifier: CA1522111505

Gene: SLC9A3

Linked Data

• dbSNP Id: rs1739297445
• gnomAD v4: 5-483176-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.483176C>T , CM000667.2:g.483176C>T	GRCh38
NC_000005.9:g.483291C>T , CM000667.1:g.483291C>T	GRCh37
NC_000005.8:g.536291C>T	NCBI36
NG_046804.1:g.92253G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264938.8:c.1153+86G>A MANE Select	ENSP00000264938.3:n.1153+86G>A
ENST00000644203.1:c.1153+86G>A	ENSP00000495903.1:n.1153+86G>A
ENST00000264938.7:c.1153+86G>A	ENSP00000264938.3:n.1153+86G>A
ENST00000514375.1:c.1153+86G>A	ENSP00000422983.1:n.1153+86G>A
NM_001284351.1:c.1153+86G>A	NP_001271280.1:n.1153+86G>A
NM_004174.2:c.1153+86G>A	NP_004165.2:n.1153+86G>A
XM_011514095.1:c.1159+86G>A	XP_011512397.1:n.1159+86G>A
XM_011514096.1:c.1153+86G>A	XP_011512398.1:n.1153+86G>A
XM_011514097.1:c.1159+86G>A	XP_011512399.1:n.1159+86G>A
XM_011514098.1:c.1159+86G>A	XP_011512400.1:n.1159+86G>A
NM_001284351.2:c.1153+86G>A	NP_001271280.1:n.1153+86G>A
NM_004174.3:c.1153+86G>A	NP_004165.2:n.1153+86G>A
NM_001284351.3:c.1153+86G>A	NP_001271280.1:n.1153+86G>A
NM_004174.4:c.1153+86G>A MANE Select	NP_004165.2:n.1153+86G>A