Canonical Allele Identifier: CA1407352538

Gene: SLC9A9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143286275_143286277delinsTGG , CM000665.2:g.143286275_143286277delinsTGG	GRCh38
NC_000003.11:g.143005117_143005119delinsTGG , CM000665.1:g.143005117_143005119delinsTGG	GRCh37
NC_000003.10:g.144487807_144487809delinsTGG	NCBI36
NG_017077.1:g.567255_567257delinsCCA
NG_017077.2:g.567255_567257delinsCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.1605-17297_1605-17295delinsCCA MANE Select	ENSP00000320246.6:n.1605-17297_1605-17295delinsCCA
ENST00000316549.10:c.1605-17297_1605-17295delinsCCA	ENSP00000320246.6:n.1605-17297_1605-17295delinsCCA
NM_173653.3:c.1605-17297_1605-17295delinsCCA	NP_775924.1:n.1605-17297_1605-17295delinsCCA
XM_011512703.1:c.957-17297_957-17295delinsCCA	XP_011511005.1:n.957-17297_957-17295delinsCCA
XM_011512703.3:c.957-17297_957-17295delinsCCA	XP_011511005.1:n.957-17297_957-17295delinsCCA
XM_017006202.2:c.1712-1935_1712-1933delinsCCA	XP_016861691.1:n.1712-1935_1712-1933delinsCCA
XM_017006203.1:c.1254-17297_1254-17295delinsCCA	XP_016861692.1:n.1254-17297_1254-17295delinsCCA
NM_173653.4:c.1605-17297_1605-17295delinsCCA MANE Select	NP_775924.1:n.1605-17297_1605-17295delinsCCA