Canonical Allele Identifier: CA2341138262

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908397A= , CM000681.2:g.50908397A=	GRCh38
NC_000019.9:g.51411653A= , CM000681.1:g.51411653A=	GRCh37
NC_000019.8:g.56103465A=	NCBI36
NG_012154.2:g.7342T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.574T= MANE Select	ENSP00000326159.1:p.Cys192=
ENST00000324041.5:c.574T=	ENSP00000326159.1:p.Cys192=
ENST00000431178.2:c.328+182T=	ENSP00000399448.2:n.328+182T=
ENST00000593885.1:c.*69T=	ENSP00000469769.1:n.*69T=
ENST00000596876.1:n.576T=
ENST00000598305.5:c.*69T=	ENSP00000469963.1:n.*69T=
ENST00000599865.5:n.510T=
ENST00000602148.1:c.586T=	ENSP00000472091.1:n.586T=
NM_001302961.1:c.289T=	NP_001289890.1:p.Cys97=
NM_004917.4:c.574T=	NP_004908.4:p.Cys192=
NR_126566.1:n.563T=
XM_005259441.3:c.289T=	XP_005259498.2:p.Cys97=
XM_011527545.1:c.*69T=	XP_011525847.1:n.*69T=
XM_011527546.1:c.475+182T=	XP_011525848.1:n.475+182T=
XM_011527547.1:c.427T=	XP_011525849.1:p.Cys143=
XM_005259441.4:c.289T=	XP_005259498.2:p.Cys97=
XM_011527545.3:c.*69T=	XP_011525847.1:n.*69T=
XM_011527546.2:c.475+182T=	XP_011525848.1:n.475+182T=
NM_001302961.2:c.289T=	NP_001289890.1:p.Cys97=
NR_126566.2:n.563T=
NM_004917.5:c.574T= MANE Select	NP_004908.4:p.Cys192=