Canonical Allele Identifier: CA359027692

Gene: SLC9A3

Linked Data

• MyVariant Identifiers: chr5:g.483397A>G (hg19) ; chr5:g.483282A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.483282A>G , CM000667.2:g.483282A>G	GRCh38
NC_000005.9:g.483397A>G , CM000667.1:g.483397A>G	GRCh37
NC_000005.8:g.536397A>G	NCBI36
NG_046804.1:g.92147T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264938.8:c.1133T>C MANE Select	ENSP00000264938.3:p.Ile378Thr
ENST00000644203.1:c.1133T>C	ENSP00000495903.1:p.Ile378Thr
ENST00000264938.7:c.1133T>C	ENSP00000264938.3:p.Ile378Thr
ENST00000514375.1:c.1133T>C	ENSP00000422983.1:p.Ile378Thr
NM_001284351.1:c.1133T>C	NP_001271280.1:p.Ile378Thr
NM_004174.2:c.1133T>C	NP_004165.2:p.Ile378Thr
XM_011514095.1:c.1139T>C	XP_011512397.1:p.Ile380Thr
XM_011514096.1:c.1133T>C	XP_011512398.1:p.Ile378Thr
XM_011514097.1:c.1139T>C	XP_011512399.1:p.Ile380Thr
XM_011514098.1:c.1139T>C	XP_011512400.1:p.Ile380Thr
NM_001284351.2:c.1133T>C	NP_001271280.1:p.Ile378Thr
NM_004174.3:c.1133T>C	NP_004165.2:p.Ile378Thr
NM_001284351.3:c.1133T>C	NP_001271280.1:p.Ile378Thr
NM_004174.4:c.1133T>C MANE Select	NP_004165.2:p.Ile378Thr