Canonical Allele Identifier: CA2341138439

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908761T= , CM000681.2:g.50908761T=	GRCh38
NC_000019.9:g.51412017T= , CM000681.1:g.51412017T=	GRCh37
NC_000019.8:g.56103829T=	NCBI36
NG_012154.2:g.6978A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.293A= MANE Select	ENSP00000326159.1:p.Glu98=
ENST00000324041.5:c.293A=	ENSP00000326159.1:p.Glu98=
ENST00000431178.2:c.146A=	ENSP00000399448.2:p.Glu49=
ENST00000593885.1:c.8A=	ENSP00000469769.1:p.Glu3=
ENST00000596876.1:n.212A=
ENST00000598305.5:c.8A=	ENSP00000469963.1:p.Glu3=
ENST00000599865.5:n.146A=
ENST00000602148.1:c.305A=	ENSP00000472091.1:n.305A=
NM_001302961.1:c.8A=	NP_001289890.1:p.Glu3=
NM_004917.4:c.293A=	NP_004908.4:p.Glu98=
NR_126566.1:n.286A=
XM_005259441.3:c.8A=	XP_005259498.2:p.Glu3=
XM_011527545.1:c.293A=	XP_011525847.1:p.Glu98=
XM_011527546.1:c.293A=	XP_011525848.1:p.Glu98=
XM_011527547.1:c.146A=	XP_011525849.1:p.Glu49=
XM_005259441.4:c.8A=	XP_005259498.2:p.Glu3=
XM_011527545.3:c.293A=	XP_011525847.1:p.Glu98=
XM_011527546.2:c.293A=	XP_011525848.1:p.Glu98=
NM_001302961.2:c.8A=	NP_001289890.1:p.Glu3=
NR_126566.2:n.286A=
NM_004917.5:c.293A= MANE Select	NP_004908.4:p.Glu98=