Canonical Allele Identifier: CA1407354841
Gene: SLC9A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143301939C= , CM000665.2:g.143301939C= GRCh38
NC_000003.11:g.143020781C= , CM000665.1:g.143020781C= GRCh37
NC_000003.10:g.144503471C= NCBI36
NG_017077.1:g.551593G=
NG_017077.2:g.551593G=

Transcript Alleles

HGVS Amino-acid change
ENST00000316549.11:c.1605-32959G= MANE Select ENSP00000320246.6:n.1605-32959G=
ENST00000316549.10:c.1605-32959G= ENSP00000320246.6:n.1605-32959G=
NM_173653.3:c.1605-32959G= NP_775924.1:n.1605-32959G=
XM_011512703.1:c.957-32959G= XP_011511005.1:n.957-32959G=
XM_011512703.3:c.957-32959G= XP_011511005.1:n.957-32959G=
XM_017006202.2:c.1712-17597G= XP_016861691.1:n.1712-17597G=
XM_017006203.1:c.1254-32959G= XP_016861692.1:n.1254-32959G=
NM_173653.4:c.1605-32959G= MANE Select NP_775924.1:n.1605-32959G=