Canonical Allele Identifier: CA1407455072

Gene: SLC9A9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143531151G= , CM000665.2:g.143531151G=	GRCh38
NC_000003.11:g.143249993G= , CM000665.1:g.143249993G=	GRCh37
NC_000003.10:g.144732683G=	NCBI36
NG_017077.1:g.322381C=
NG_017077.2:g.322381C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.1089+21211C= MANE Select	ENSP00000320246.6:n.1089+21211C=
ENST00000316549.10:c.1089+21211C=	ENSP00000320246.6:n.1089+21211C=
NM_173653.3:c.1089+21211C=	NP_775924.1:n.1089+21211C=
XM_011512703.1:c.441+21211C=	XP_011511005.1:n.441+21211C=
XM_011512703.3:c.441+21211C=	XP_011511005.1:n.441+21211C=
XM_017006202.2:c.1089+21211C=	XP_016861691.1:n.1089+21211C=
XM_017006203.1:c.738+21211C=	XP_016861692.1:n.738+21211C=
NM_173653.4:c.1089+21211C= MANE Select	NP_775924.1:n.1089+21211C=