Canonical Allele Identifier: CA2341138473

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908822T= , CM000681.2:g.50908822T=	GRCh38
NC_000019.9:g.51412078T= , CM000681.1:g.51412078T=	GRCh37
NC_000019.8:g.56103890T=	NCBI36
NG_012154.2:g.6917A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000324041.6:c.232A= MANE Select	ENSP00000326159.1:p.Thr78=
ENST00000324041.5:c.232A=	ENSP00000326159.1:p.Thr78=
ENST00000431178.2:c.85A=	ENSP00000399448.2:p.Thr29=
ENST00000593885.1:c.-54A=	ENSP00000469769.1:n.-54A=
ENST00000596876.1:n.151A=
ENST00000598305.5:c.-54A=	ENSP00000469963.1:n.-54A=
ENST00000599865.5:n.85A=
ENST00000602148.1:c.244A=	ENSP00000472091.1:n.244A=
NM_001302961.1:c.-54A=	NP_001289890.1:n.-54A=
NM_004917.4:c.232A=	NP_004908.4:p.Thr78=
NR_126566.1:n.225A=
XM_005259441.3:c.-54A=	XP_005259498.2:n.-54A=
XM_011527545.1:c.232A=	XP_011525847.1:p.Thr78=
XM_011527546.1:c.232A=	XP_011525848.1:p.Thr78=
XM_011527547.1:c.85A=	XP_011525849.1:p.Thr29=
XM_005259441.4:c.-54A=	XP_005259498.2:n.-54A=
XM_011527545.3:c.232A=	XP_011525847.1:p.Thr78=
XM_011527546.2:c.232A=	XP_011525848.1:p.Thr78=
NM_001302961.2:c.-54A=	NP_001289890.1:n.-54A=
NR_126566.2:n.225A=
NM_004917.5:c.232A= MANE Select	NP_004908.4:p.Thr78=