Canonical Allele Identifier: CA1407354906

Gene: SLC9A9

Linked Data

• dbSNP Id: rs2030547603

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143302093_143302099del , CM000665.2:g.143302093_143302099del	GRCh38
NC_000003.11:g.143020935_143020941del , CM000665.1:g.143020935_143020941del	GRCh37
NC_000003.10:g.144503625_144503631del	NCBI36
NG_017077.1:g.551433_551439del
NG_017077.2:g.551433_551439del

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.1605-33119_1605-33113del MANE Select	ENSP00000320246.6:n.1605-33119_1605-33113...
ENST00000316549.10:c.1605-33119_1605-33113del	ENSP00000320246.6:n.1605-33119_1605-33113...
NM_173653.3:c.1605-33119_1605-33113del	NP_775924.1:n.1605-33119_1605-33113del
XM_011512703.1:c.957-33119_957-33113del	XP_011511005.1:n.957-33119_957-33113del
XM_011512703.3:c.957-33119_957-33113del	XP_011511005.1:n.957-33119_957-33113del
XM_017006202.2:c.1712-17757_1712-17751del	XP_016861691.1:n.1712-17757_1712-17751del...
XM_017006203.1:c.1254-33119_1254-33113del	XP_016861692.1:n.1254-33119_1254-33113del...
NM_173653.4:c.1605-33119_1605-33113del MANE Select	NP_775924.1:n.1605-33119_1605-33113del