Canonical Allele Identifier: CA1407372393

Gene: SLC9A9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143337668T= , CM000665.2:g.143337668T=	GRCh38
NC_000003.11:g.143056510T= , CM000665.1:g.143056510T=	GRCh37
NC_000003.10:g.144539200T=	NCBI36
NG_017077.1:g.515864A=
NG_017077.2:g.515864A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.1604+25816A= MANE Select	ENSP00000320246.6:n.1604+25816A=
ENST00000316549.10:c.1604+25816A=	ENSP00000320246.6:n.1604+25816A=
NM_173653.3:c.1604+25816A=	NP_775924.1:n.1604+25816A=
XM_011512703.1:c.956+25816A=	XP_011511005.1:n.956+25816A=
XM_011512703.3:c.956+25816A=	XP_011511005.1:n.956+25816A=
XM_017006202.2:c.1711+25709A=	XP_016861691.1:n.1711+25709A=
XM_017006203.1:c.1253+25816A=	XP_016861692.1:n.1253+25816A=
NM_173653.4:c.1604+25816A= MANE Select	NP_775924.1:n.1604+25816A=