Canonical Allele Identifier: CA1407571647

Gene: SLC9A9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143785725T= , CM000665.2:g.143785725T=	GRCh38
NC_000003.11:g.143504567T= , CM000665.1:g.143504567T=	GRCh37
NC_000003.10:g.144987257T=	NCBI36
NG_017077.1:g.67807A=
NG_017077.2:g.67807A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.533+9276A= MANE Select	ENSP00000320246.6:n.533+9276A=
ENST00000316549.10:c.533+9276A=	ENSP00000320246.6:n.533+9276A=
ENST00000474727.2:c.*144+9276A=	ENSP00000419090.2:n.*144+9276A=
NM_173653.3:c.533+9276A=	NP_775924.1:n.533+9276A=
XM_011512704.1:c.533+9276A=	XP_011511006.1:n.533+9276A=
XM_011512704.3:c.533+9276A=	XP_011511006.1:n.533+9276A=
XM_017006202.2:c.533+9276A=	XP_016861691.1:n.533+9276A=
XM_017006203.1:c.182+9276A=	XP_016861692.1:n.182+9276A=
NM_173653.4:c.533+9276A= MANE Select	NP_775924.1:n.533+9276A=