Canonical Allele Identifier: CA3176277

Gene: SLC9A3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.488373G>A , CM000667.2:g.488373G>A	GRCh38
NC_000005.9:g.488488G>A , CM000667.1:g.488488G>A	GRCh37
NC_000005.8:g.541488G>A	NCBI36
NG_046804.1:g.87056C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004174.4:c.618C>T MANE Select	NP_004165.2:p.Asn206=
ENST00000264938.8:c.618C>T MANE Select	ENSP00000264938.3:p.Asn206=
NM_001284351.1:c.618C>T	NP_001271280.1:p.Asn206=
NM_001284351.2:c.618C>T	NP_001271280.1:p.Asn206=
NM_001284351.3:c.618C>T	NP_001271280.1:p.Asn206=
NM_004174.2:c.618C>T	NP_004165.2:p.Asn206=
NM_004174.3:c.618C>T	NP_004165.2:p.Asn206=
ENST00000264938.7:c.618C>T	ENSP00000264938.3:p.Asn206=
ENST00000514375.1:c.618C>T	ENSP00000422983.1:p.Asn206=
ENST00000644203.1:c.618C>T	ENSP00000495903.1:p.Asn206=
XM_011514095.1:c.624C>T	XP_011512397.1:p.Asn208=
XM_011514096.1:c.618C>T	XP_011512398.1:p.Asn206=
XM_011514097.1:c.624C>T	XP_011512399.1:p.Asn208=
XM_011514098.1:c.624C>T	XP_011512400.1:p.Asn208=