Canonical Allele Identifier: CA1407354850
Gene: SLC9A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143301966_143301968delinsAAG , CM000665.2:g.143301966_143301968delinsAAG GRCh38
NC_000003.11:g.143020808_143020810delinsAAG , CM000665.1:g.143020808_143020810delinsAAG GRCh37
NC_000003.10:g.144503498_144503500delinsAAG NCBI36
NG_017077.1:g.551564_551566delinsCTT
NG_017077.2:g.551564_551566delinsCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000316549.11:c.1605-32988_1605-32986delinsCTT MANE Select ENSP00000320246.6:n.1605-32988_1605-32986...
ENST00000316549.10:c.1605-32988_1605-32986delinsCTT ENSP00000320246.6:n.1605-32988_1605-32986...
NM_173653.3:c.1605-32988_1605-32986delinsCTT NP_775924.1:n.1605-32988_1605-32986delins...
XM_011512703.1:c.957-32988_957-32986delinsCTT XP_011511005.1:n.957-32988_957-32986delin...
XM_011512703.3:c.957-32988_957-32986delinsCTT XP_011511005.1:n.957-32988_957-32986delin...
XM_017006202.2:c.1712-17626_1712-17624delinsCTT XP_016861691.1:n.1712-17626_1712-17624del...
XM_017006203.1:c.1254-32988_1254-32986delinsCTT XP_016861692.1:n.1254-32988_1254-32986del...
NM_173653.4:c.1605-32988_1605-32986delinsCTT MANE Select NP_775924.1:n.1605-32988_1605-32986delins...