Canonical Allele Identifier: CA2341138440

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908762C= , CM000681.2:g.50908762C=	GRCh38
NC_000019.9:g.51412018C= , CM000681.1:g.51412018C=	GRCh37
NC_000019.8:g.56103830C=	NCBI36
NG_012154.2:g.6977G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.292G= MANE Select	ENSP00000326159.1:p.Glu98=
ENST00000324041.5:c.292G=	ENSP00000326159.1:p.Glu98=
ENST00000431178.2:c.145G=	ENSP00000399448.2:p.Glu49=
ENST00000593885.1:c.7G=	ENSP00000469769.1:p.Glu3=
ENST00000596876.1:n.211G=
ENST00000598305.5:c.7G=	ENSP00000469963.1:p.Glu3=
ENST00000599865.5:n.145G=
ENST00000602148.1:c.304G=	ENSP00000472091.1:n.304G=
NM_001302961.1:c.7G=	NP_001289890.1:p.Glu3=
NM_004917.4:c.292G=	NP_004908.4:p.Glu98=
NR_126566.1:n.285G=
XM_005259441.3:c.7G=	XP_005259498.2:p.Glu3=
XM_011527545.1:c.292G=	XP_011525847.1:p.Glu98=
XM_011527546.1:c.292G=	XP_011525848.1:p.Glu98=
XM_011527547.1:c.145G=	XP_011525849.1:p.Glu49=
XM_005259441.4:c.7G=	XP_005259498.2:p.Glu3=
XM_011527545.3:c.292G=	XP_011525847.1:p.Glu98=
XM_011527546.2:c.292G=	XP_011525848.1:p.Glu98=
NM_001302961.2:c.7G=	NP_001289890.1:p.Glu3=
NR_126566.2:n.285G=
NM_004917.5:c.292G= MANE Select	NP_004908.4:p.Glu98=