Canonical Allele Identifier: CA900065619

Gene: SLC9A9

Linked Data

• dbSNP Id: rs1410138010
• MyVariant Identifiers: chr3:g.143504583G>A (hg19) ; chr3:g.143785741G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143785741G>A , CM000665.2:g.143785741G>A	GRCh38
NC_000003.11:g.143504583G>A , CM000665.1:g.143504583G>A	GRCh37
NC_000003.10:g.144987273G>A	NCBI36
NG_017077.1:g.67791C>T
NG_017077.2:g.67791C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.533+9260C>T MANE Select	ENSP00000320246.6:n.533+9260C>T
ENST00000316549.10:c.533+9260C>T	ENSP00000320246.6:n.533+9260C>T
ENST00000474727.2:c.*144+9260C>T	ENSP00000419090.2:n.*144+9260C>T
NM_173653.3:c.533+9260C>T	NP_775924.1:n.533+9260C>T
XM_011512704.1:c.533+9260C>T	XP_011511006.1:n.533+9260C>T
XM_011512704.3:c.533+9260C>T	XP_011511006.1:n.533+9260C>T
XM_017006202.2:c.533+9260C>T	XP_016861691.1:n.533+9260C>T
XM_017006203.1:c.182+9260C>T	XP_016861692.1:n.182+9260C>T
NM_173653.4:c.533+9260C>T MANE Select	NP_775924.1:n.533+9260C>T