Canonical Allele Identifier: CA2526136640

Gene: SLC9A9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143286258_143286259insATGGCA , CM000665.2:g.143286258_143286259insATGGCA	GRCh38
NC_000003.11:g.143005100_143005101insATGGCA , CM000665.1:g.143005100_143005101insATGGCA	GRCh37
NC_000003.10:g.144487790_144487791insATGGCA	NCBI36
NG_017077.1:g.567273_567274insTGCCAT
NG_017077.2:g.567273_567274insTGCCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.1605-17279_1605-17278insTGCCAT MANE Select	ENSP00000320246.6:n.1605-17279_1605-17278insTGCCAT
ENST00000316549.10:c.1605-17279_1605-17278insTGCCAT	ENSP00000320246.6:n.1605-17279_1605-17278insTGCCAT
NM_173653.3:c.1605-17279_1605-17278insTGCCAT	NP_775924.1:n.1605-17279_1605-17278insTGCCAT
XM_011512703.1:c.957-17279_957-17278insTGCCAT	XP_011511005.1:n.957-17279_957-17278insTGCCAT
XM_011512703.3:c.957-17279_957-17278insTGCCAT	XP_011511005.1:n.957-17279_957-17278insTGCCAT
XM_017006202.2:c.1712-1917_1712-1916insTGCCAT	XP_016861691.1:n.1712-1917_1712-1916insTGCCAT
XM_017006203.1:c.1254-17279_1254-17278insTGCCAT	XP_016861692.1:n.1254-17279_1254-17278insTGCCAT
NM_173653.4:c.1605-17279_1605-17278insTGCCAT MANE Select	NP_775924.1:n.1605-17279_1605-17278insTGCCAT