Canonical Allele Identifier: CA2341138401
Gene: KLK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908674G= , CM000681.2:g.50908674G= GRCh38
NC_000019.9:g.51411930G= , CM000681.1:g.51411930G= GRCh37
NC_000019.8:g.56103742G= NCBI36
NG_012154.2:g.7065C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.380C= MANE Select ENSP00000326159.1:p.Ser127=
ENST00000324041.5:c.380C= ENSP00000326159.1:p.Ser127=
ENST00000431178.2:c.233C= ENSP00000399448.2:p.Ser78=
ENST00000593885.1:c.95C= ENSP00000469769.1:p.Ser32=
ENST00000596876.1:n.299C=
ENST00000598305.5:c.95C= ENSP00000469963.1:p.Ser32=
ENST00000599865.5:n.233C=
ENST00000602148.1:c.392C= ENSP00000472091.1:n.392C=
NM_001302961.1:c.95C= NP_001289890.1:p.Ser32=
NM_004917.4:c.380C= NP_004908.4:p.Ser127=
NR_126566.1:n.373C=
XM_005259441.3:c.95C= XP_005259498.2:p.Ser32=
XM_011527545.1:c.380C= XP_011525847.1:p.Ser127=
XM_011527546.1:c.380C= XP_011525848.1:p.Ser127=
XM_011527547.1:c.233C= XP_011525849.1:p.Ser78=
XM_005259441.4:c.95C= XP_005259498.2:p.Ser32=
XM_011527545.3:c.380C= XP_011525847.1:p.Ser127=
XM_011527546.2:c.380C= XP_011525848.1:p.Ser127=
NM_001302961.2:c.95C= NP_001289890.1:p.Ser32=
NR_126566.2:n.373C=
NM_004917.5:c.380C= MANE Select NP_004908.4:p.Ser127=