Canonical Allele Identifier: CA1407536514

Gene: SLC9A9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143707086_143707088delinsGGA , CM000665.2:g.143707086_143707088delinsGGA	GRCh38
NC_000003.11:g.143425928_143425930delinsGGA , CM000665.1:g.143425928_143425930delinsGGA	GRCh37
NC_000003.10:g.144908618_144908620delinsGGA	NCBI36
NG_017077.1:g.146444_146446delinsTCC
NG_017077.2:g.146444_146446delinsTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.534-13781_534-13779delinsTCC MANE Select	ENSP00000320246.6:n.534-13781_534-13779delinsTCC
ENST00000316549.10:c.534-13781_534-13779delinsTCC	ENSP00000320246.6:n.534-13781_534-13779delinsTCC
ENST00000474727.2:c.*145-13781_*145-13779delinsTCC	ENSP00000419090.2:n.*145-13781_*145-13779delinsTCC
NM_173653.3:c.534-13781_534-13779delinsTCC	NP_775924.1:n.534-13781_534-13779delinsTCC
XM_011512704.1:c.534-13781_534-13779delinsTCC	XP_011511006.1:n.534-13781_534-13779delinsTCC
XM_011512704.3:c.534-13781_534-13779delinsTCC	XP_011511006.1:n.534-13781_534-13779delinsTCC
XM_017006202.2:c.534-13781_534-13779delinsTCC	XP_016861691.1:n.534-13781_534-13779delinsTCC
XM_017006203.1:c.183-13781_183-13779delinsTCC	XP_016861692.1:n.183-13781_183-13779delinsTCC
NM_173653.4:c.534-13781_534-13779delinsTCC MANE Select	NP_775924.1:n.534-13781_534-13779delinsTCC