Canonical Allele Identifier: CA1407352450
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs1938374432

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143286110del , CM000665.2:g.143286110del GRCh38
NC_000003.11:g.143004952del , CM000665.1:g.143004952del GRCh37
NC_000003.10:g.144487642del NCBI36
NG_017077.1:g.567423del
NG_017077.2:g.567423del

Transcript Alleles

HGVS Amino-acid change
ENST00000316549.11:c.1605-17129del MANE Select ENSP00000320246.6:n.1605-17129del
ENST00000316549.10:c.1605-17129del ENSP00000320246.6:n.1605-17129del
NM_173653.3:c.1605-17129del NP_775924.1:n.1605-17129del
XM_011512703.1:c.957-17129del XP_011511005.1:n.957-17129del
XM_011512703.3:c.957-17129del XP_011511005.1:n.957-17129del
XM_017006202.2:c.1712-1767del XP_016861691.1:n.1712-1767del
XM_017006203.1:c.1254-17129del XP_016861692.1:n.1254-17129del
NM_173653.4:c.1605-17129del MANE Select NP_775924.1:n.1605-17129del