Canonical Allele Identifier: CA3006081494
Gene: KLK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908478_50908480del , CM000681.2:g.50908478_50908480del GRCh38
NC_000019.9:g.51411734_51411736del , CM000681.1:g.51411734_51411736del GRCh37
NC_000019.8:g.56103546_56103548del NCBI36
NG_012154.2:g.7262_7264del

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.494_496del MANE Select ENSP00000326159.1:p.Leu165del
ENST00000324041.5:c.494_496del ENSP00000326159.1:p.Leu165del
ENST00000431178.2:c.328+102_328+104del ENSP00000399448.2:n.328+102_328+104del
ENST00000593885.1:c.205_207del ENSP00000469769.1:p.Cys69del
ENST00000596876.1:n.496_498del
ENST00000598305.5:c.205_207del ENSP00000469963.1:p.Cys69del
ENST00000599865.5:n.430_432del
ENST00000602148.1:c.506_508del ENSP00000472091.1:n.506_508del
NM_001302961.1:c.209_211del NP_001289890.1:p.Leu70del
NM_004917.4:c.494_496del NP_004908.4:p.Leu165del
NR_126566.1:n.483_485del
XM_005259441.3:c.209_211del XP_005259498.2:p.Leu70del
XM_011527545.1:c.490_492del XP_011525847.1:p.Cys164del
XM_011527546.1:c.475+102_475+104del XP_011525848.1:n.475+102_475+104del
XM_011527547.1:c.347_349del XP_011525849.1:p.Leu116del
XM_005259441.4:c.209_211del XP_005259498.2:p.Leu70del
XM_011527545.3:c.490_492del XP_011525847.1:p.Cys164del
XM_011527546.2:c.475+102_475+104del XP_011525848.1:n.475+102_475+104del
NM_001302961.2:c.209_211del NP_001289890.1:p.Leu70del
NR_126566.2:n.483_485del
NM_004917.5:c.494_496del MANE Select NP_004908.4:p.Leu165del