Canonical Allele Identifier: CA1522111614

Gene: SLC9A3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.483277C= , CM000667.2:g.483277C=	GRCh38
NC_000005.9:g.483392C= , CM000667.1:g.483392C=	GRCh37
NC_000005.8:g.536392C=	NCBI36
NG_046804.1:g.92152G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264938.8:c.1138G= MANE Select	ENSP00000264938.3:p.Val380=
ENST00000644203.1:c.1138G=	ENSP00000495903.1:p.Val380=
ENST00000264938.7:c.1138G=	ENSP00000264938.3:p.Val380=
ENST00000514375.1:c.1138G=	ENSP00000422983.1:p.Val380=
NM_001284351.1:c.1138G=	NP_001271280.1:p.Val380=
NM_004174.2:c.1138G=	NP_004165.2:p.Val380=
XM_011514095.1:c.1144G=	XP_011512397.1:p.Val382=
XM_011514096.1:c.1138G=	XP_011512398.1:p.Val380=
XM_011514097.1:c.1144G=	XP_011512399.1:p.Val382=
XM_011514098.1:c.1144G=	XP_011512400.1:p.Val382=
NM_001284351.2:c.1138G=	NP_001271280.1:p.Val380=
NM_004174.3:c.1138G=	NP_004165.2:p.Val380=
NM_001284351.3:c.1138G=	NP_001271280.1:p.Val380=
NM_004174.4:c.1138G= MANE Select	NP_004165.2:p.Val380=