Canonical Allele Identifier: CA2341138269
Gene: KLK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908416C= , CM000681.2:g.50908416C= GRCh38
NC_000019.9:g.51411672C= , CM000681.1:g.51411672C= GRCh37
NC_000019.8:g.56103484C= NCBI36
NG_012154.2:g.7323G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.555G= MANE Select ENSP00000326159.1:p.Leu185=
ENST00000324041.5:c.555G= ENSP00000326159.1:p.Leu185=
ENST00000431178.2:c.328+163G= ENSP00000399448.2:n.328+163G=
ENST00000593885.1:c.*50G= ENSP00000469769.1:n.*50G=
ENST00000596876.1:n.557G=
ENST00000598305.5:c.*50G= ENSP00000469963.1:n.*50G=
ENST00000599865.5:n.491G=
ENST00000602148.1:c.567G= ENSP00000472091.1:n.567G=
NM_001302961.1:c.270G= NP_001289890.1:p.Leu90=
NM_004917.4:c.555G= NP_004908.4:p.Leu185=
NR_126566.1:n.544G=
XM_005259441.3:c.270G= XP_005259498.2:p.Leu90=
XM_011527545.1:c.*50G= XP_011525847.1:n.*50G=
XM_011527546.1:c.475+163G= XP_011525848.1:n.475+163G=
XM_011527547.1:c.408G= XP_011525849.1:p.Leu136=
XM_005259441.4:c.270G= XP_005259498.2:p.Leu90=
XM_011527545.3:c.*50G= XP_011525847.1:n.*50G=
XM_011527546.2:c.475+163G= XP_011525848.1:n.475+163G=
NM_001302961.2:c.270G= NP_001289890.1:p.Leu90=
NR_126566.2:n.544G=
NM_004917.5:c.555G= MANE Select NP_004908.4:p.Leu185=