Canonical Allele Identifier: CA2586648216
Gene: KLK4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908565_50908566del , CM000681.2:g.50908565_50908566del GRCh38
NC_000019.9:g.51411821_51411822del , CM000681.1:g.51411821_51411822del GRCh37
NC_000019.8:g.56103633_56103634del NCBI36
NG_012154.2:g.7179_7180del

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.475+19_475+20del MANE Select ENSP00000326159.1:n.475+19_475+20del
ENST00000324041.5:c.475+19_475+20del ENSP00000326159.1:n.475+19_475+20del
ENST00000431178.2:c.328+19_328+20del ENSP00000399448.2:n.328+19_328+20del
ENST00000593885.1:c.190+19_190+20del ENSP00000469769.1:n.190+19_190+20del
ENST00000596876.1:n.413_414del
ENST00000598305.5:c.190+19_190+20del ENSP00000469963.1:n.190+19_190+20del
ENST00000599865.5:n.347_348del
ENST00000602148.1:c.487+19_487+20del ENSP00000472091.1:n.487+19_487+20del
NM_001302961.1:c.190+19_190+20del NP_001289890.1:n.190+19_190+20del
NM_004917.4:c.475+19_475+20del NP_004908.4:n.475+19_475+20del
NR_126566.1:n.468+19_468+20del
XM_005259441.3:c.190+19_190+20del XP_005259498.2:n.190+19_190+20del
XM_011527545.1:c.475+19_475+20del XP_011525847.1:n.475+19_475+20del
XM_011527546.1:c.475+19_475+20del XP_011525848.1:n.475+19_475+20del
XM_011527547.1:c.328+19_328+20del XP_011525849.1:n.328+19_328+20del
XM_005259441.4:c.190+19_190+20del XP_005259498.2:n.190+19_190+20del
XM_011527545.3:c.475+19_475+20del XP_011525847.1:n.475+19_475+20del
XM_011527546.2:c.475+19_475+20del XP_011525848.1:n.475+19_475+20del
NM_001302961.2:c.190+19_190+20del NP_001289890.1:n.190+19_190+20del
NR_126566.2:n.468+19_468+20del
NM_004917.5:c.475+19_475+20del MANE Select NP_004908.4:n.475+19_475+20del