Canonical Allele Identifier: CA1407455102

Gene: SLC9A9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143531198_143531211delinsTACATCAACTCATG , CM000665.2:g.143531198_143531211delinsTACATCAACTCATG	GRCh38
NC_000003.11:g.143250040_143250053delinsTACATCAACTCATG , CM000665.1:g.143250040_143250053delinsTACATCAACTCATG	GRCh37
NC_000003.10:g.144732730_144732743delinsTACATCAACTCATG	NCBI36
NG_017077.1:g.322321_322334delinsCATGAGTTGATGTA
NG_017077.2:g.322321_322334delinsCATGAGTTGATGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.1089+21151_1089+21164delinsCATGAGTTGATGTA MANE Select	ENSP00000320246.6:n.1089+21151_1089+21164delinsCATGAGTTGATGTA...
ENST00000316549.10:c.1089+21151_1089+21164delinsCATGAGTTGATGTA	ENSP00000320246.6:n.1089+21151_1089+21164delinsCATGAGTTGATGTA...
NM_173653.3:c.1089+21151_1089+21164delinsCATGAGTTGATGTA	NP_775924.1:n.1089+21151_1089+21164delinsCATGAGTTGATGTA
XM_011512703.1:c.441+21151_441+21164delinsCATGAGTTGATGTA	XP_011511005.1:n.441+21151_441+21164delinsCATGAGTTGATGTA
XM_011512703.3:c.441+21151_441+21164delinsCATGAGTTGATGTA	XP_011511005.1:n.441+21151_441+21164delinsCATGAGTTGATGTA
XM_017006202.2:c.1089+21151_1089+21164delinsCATGAGTTGATGTA	XP_016861691.1:n.1089+21151_1089+21164delinsCATGAGTTGATGTA
XM_017006203.1:c.738+21151_738+21164delinsCATGAGTTGATGTA	XP_016861692.1:n.738+21151_738+21164delinsCATGAGTTGATGTA
NM_173653.4:c.1089+21151_1089+21164delinsCATGAGTTGATGTA MANE Select	NP_775924.1:n.1089+21151_1089+21164delinsCATGAGTTGATGTA