Canonical Allele Identifier: CA2673001844

Gene: SLC9A3

Linked Data

• gnomAD v4: 5-483188-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.483188A>G , CM000667.2:g.483188A>G	GRCh38
NC_000005.9:g.483303A>G , CM000667.1:g.483303A>G	GRCh37
NC_000005.8:g.536303A>G	NCBI36
NG_046804.1:g.92241T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264938.8:c.1153+74T>C MANE Select	ENSP00000264938.3:n.1153+74T>C
ENST00000644203.1:c.1153+74T>C	ENSP00000495903.1:n.1153+74T>C
ENST00000264938.7:c.1153+74T>C	ENSP00000264938.3:n.1153+74T>C
ENST00000514375.1:c.1153+74T>C	ENSP00000422983.1:n.1153+74T>C
NM_001284351.1:c.1153+74T>C	NP_001271280.1:n.1153+74T>C
NM_004174.2:c.1153+74T>C	NP_004165.2:n.1153+74T>C
XM_011514095.1:c.1159+74T>C	XP_011512397.1:n.1159+74T>C
XM_011514096.1:c.1153+74T>C	XP_011512398.1:n.1153+74T>C
XM_011514097.1:c.1159+74T>C	XP_011512399.1:n.1159+74T>C
XM_011514098.1:c.1159+74T>C	XP_011512400.1:n.1159+74T>C
NM_001284351.2:c.1153+74T>C	NP_001271280.1:n.1153+74T>C
NM_004174.3:c.1153+74T>C	NP_004165.2:n.1153+74T>C
NM_001284351.3:c.1153+74T>C	NP_001271280.1:n.1153+74T>C
NM_004174.4:c.1153+74T>C MANE Select	NP_004165.2:n.1153+74T>C