Canonical Allele Identifier: CA1407455078

Gene: SLC9A9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143531160_143531161delinsTA , CM000665.2:g.143531160_143531161delinsTA	GRCh38
NC_000003.11:g.143250002_143250003delinsTA , CM000665.1:g.143250002_143250003delinsTA	GRCh37
NC_000003.10:g.144732692_144732693delinsTA	NCBI36
NG_017077.1:g.322371_322372delinsTA
NG_017077.2:g.322371_322372delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.1089+21201_1089+21202delinsTA MANE Select	ENSP00000320246.6:n.1089+21201_1089+21202delinsTA
ENST00000316549.10:c.1089+21201_1089+21202delinsTA	ENSP00000320246.6:n.1089+21201_1089+21202delinsTA
NM_173653.3:c.1089+21201_1089+21202delinsTA	NP_775924.1:n.1089+21201_1089+21202delinsTA
XM_011512703.1:c.441+21201_441+21202delinsTA	XP_011511005.1:n.441+21201_441+21202delinsTA
XM_011512703.3:c.441+21201_441+21202delinsTA	XP_011511005.1:n.441+21201_441+21202delinsTA
XM_017006202.2:c.1089+21201_1089+21202delinsTA	XP_016861691.1:n.1089+21201_1089+21202delinsTA
XM_017006203.1:c.738+21201_738+21202delinsTA	XP_016861692.1:n.738+21201_738+21202delinsTA
NM_173653.4:c.1089+21201_1089+21202delinsTA MANE Select	NP_775924.1:n.1089+21201_1089+21202delinsTA