Canonical Allele Identifier: CA2673001812

Gene: SLC9A3

Linked Data

• gnomAD v4: 5-483180-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.483180G>A , CM000667.2:g.483180G>A	GRCh38
NC_000005.9:g.483295G>A , CM000667.1:g.483295G>A	GRCh37
NC_000005.8:g.536295G>A	NCBI36
NG_046804.1:g.92249C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264938.8:c.1153+82C>T MANE Select	ENSP00000264938.3:n.1153+82C>T
ENST00000644203.1:c.1153+82C>T	ENSP00000495903.1:n.1153+82C>T
ENST00000264938.7:c.1153+82C>T	ENSP00000264938.3:n.1153+82C>T
ENST00000514375.1:c.1153+82C>T	ENSP00000422983.1:n.1153+82C>T
NM_001284351.1:c.1153+82C>T	NP_001271280.1:n.1153+82C>T
NM_004174.2:c.1153+82C>T	NP_004165.2:n.1153+82C>T
XM_011514095.1:c.1159+82C>T	XP_011512397.1:n.1159+82C>T
XM_011514096.1:c.1153+82C>T	XP_011512398.1:n.1153+82C>T
XM_011514097.1:c.1159+82C>T	XP_011512399.1:n.1159+82C>T
XM_011514098.1:c.1159+82C>T	XP_011512400.1:n.1159+82C>T
NM_001284351.2:c.1153+82C>T	NP_001271280.1:n.1153+82C>T
NM_004174.3:c.1153+82C>T	NP_004165.2:n.1153+82C>T
NM_001284351.3:c.1153+82C>T	NP_001271280.1:n.1153+82C>T
NM_004174.4:c.1153+82C>T MANE Select	NP_004165.2:n.1153+82C>T