Canonical Allele Identifier: CA1407571658

Gene: SLC9A9

Genomic Alleles

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

Transcript Alleles

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