Canonical Allele Identifier: CA2341138264
Gene: KLK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908405C= , CM000681.2:g.50908405C= GRCh38
NC_000019.9:g.51411661C= , CM000681.1:g.51411661C= GRCh37
NC_000019.8:g.56103473C= NCBI36
NG_012154.2:g.7334G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.566G= MANE Select ENSP00000326159.1:p.Ser189=
ENST00000324041.5:c.566G= ENSP00000326159.1:p.Ser189=
ENST00000431178.2:c.328+174G= ENSP00000399448.2:n.328+174G=
ENST00000593885.1:c.*61G= ENSP00000469769.1:n.*61G=
ENST00000596876.1:n.568G=
ENST00000598305.5:c.*61G= ENSP00000469963.1:n.*61G=
ENST00000599865.5:n.502G=
ENST00000602148.1:c.578G= ENSP00000472091.1:n.578G=
NM_001302961.1:c.281G= NP_001289890.1:p.Ser94=
NM_004917.4:c.566G= NP_004908.4:p.Ser189=
NR_126566.1:n.555G=
XM_005259441.3:c.281G= XP_005259498.2:p.Ser94=
XM_011527545.1:c.*61G= XP_011525847.1:n.*61G=
XM_011527546.1:c.475+174G= XP_011525848.1:n.475+174G=
XM_011527547.1:c.419G= XP_011525849.1:p.Ser140=
XM_005259441.4:c.281G= XP_005259498.2:p.Ser94=
XM_011527545.3:c.*61G= XP_011525847.1:n.*61G=
XM_011527546.2:c.475+174G= XP_011525848.1:n.475+174G=
NM_001302961.2:c.281G= NP_001289890.1:p.Ser94=
NR_126566.2:n.555G=
NM_004917.5:c.566G= MANE Select NP_004908.4:p.Ser189=