Canonical Allele Identifier: CA2758721762
Gene: SLC9A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143337634del , CM000665.2:g.143337634del GRCh38
NC_000003.11:g.143056476del , CM000665.1:g.143056476del GRCh37
NC_000003.10:g.144539166del NCBI36
NG_017077.1:g.515898del
NG_017077.2:g.515898del

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.1604+25850del MANE Select ENSP00000320246.6:n.1604+25850del
ENST00000316549.10:c.1604+25850del ENSP00000320246.6:n.1604+25850del
NM_173653.3:c.1604+25850del NP_775924.1:n.1604+25850del
XM_011512703.1:c.956+25850del XP_011511005.1:n.956+25850del
XM_011512703.3:c.956+25850del XP_011511005.1:n.956+25850del
XM_017006202.2:c.1711+25743del XP_016861691.1:n.1711+25743del
XM_017006203.1:c.1253+25850del XP_016861692.1:n.1253+25850del
NM_173653.4:c.1604+25850del MANE Select NP_775924.1:n.1604+25850del