Canonical Allele Identifier: CA2341138377

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908625G= , CM000681.2:g.50908625G=	GRCh38
NC_000019.9:g.51411881G= , CM000681.1:g.51411881G=	GRCh37
NC_000019.8:g.56103693G=	NCBI36
NG_012154.2:g.7114C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.429C= MANE Select	ENSP00000326159.1:p.Thr143=
ENST00000324041.5:c.429C=	ENSP00000326159.1:p.Thr143=
ENST00000431178.2:c.282C=	ENSP00000399448.2:p.Thr94=
ENST00000593885.1:c.144C=	ENSP00000469769.1:p.Thr48=
ENST00000596876.1:n.348C=
ENST00000598305.5:c.144C=	ENSP00000469963.1:p.Thr48=
ENST00000599865.5:n.282C=
ENST00000602148.1:c.441C=	ENSP00000472091.1:n.441C=
NM_001302961.1:c.144C=	NP_001289890.1:p.Thr48=
NM_004917.4:c.429C=	NP_004908.4:p.Thr143=
NR_126566.1:n.422C=
XM_005259441.3:c.144C=	XP_005259498.2:p.Thr48=
XM_011527545.1:c.429C=	XP_011525847.1:p.Thr143=
XM_011527546.1:c.429C=	XP_011525848.1:p.Thr143=
XM_011527547.1:c.282C=	XP_011525849.1:p.Thr94=
XM_005259441.4:c.144C=	XP_005259498.2:p.Thr48=
XM_011527545.3:c.429C=	XP_011525847.1:p.Thr143=
XM_011527546.2:c.429C=	XP_011525848.1:p.Thr143=
NM_001302961.2:c.144C=	NP_001289890.1:p.Thr48=
NR_126566.2:n.422C=
NM_004917.5:c.429C= MANE Select	NP_004908.4:p.Thr143=