Canonical Allele Identifier: CA2341138249

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908376G= , CM000681.2:g.50908376G=	GRCh38
NC_000019.9:g.51411632G= , CM000681.1:g.51411632G=	GRCh37
NC_000019.8:g.56103444G=	NCBI36
NG_012154.2:g.7363C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.595C= MANE Select	ENSP00000326159.1:p.Gln199=
ENST00000324041.5:c.595C=	ENSP00000326159.1:p.Gln199=
ENST00000431178.2:c.328+203C=	ENSP00000399448.2:n.328+203C=
ENST00000593885.1:c.*90C=	ENSP00000469769.1:n.*90C=
ENST00000596876.1:n.597C=
ENST00000598305.5:c.*90C=	ENSP00000469963.1:n.*90C=
ENST00000599865.5:n.531C=
ENST00000602148.1:c.607C=	ENSP00000472091.1:n.607C=
NM_001302961.1:c.310C=	NP_001289890.1:p.Gln104=
NM_004917.4:c.595C=	NP_004908.4:p.Gln199=
NR_126566.1:n.584C=
XM_005259441.3:c.310C=	XP_005259498.2:p.Gln104=
XM_011527546.1:c.475+203C=	XP_011525848.1:n.475+203C=
XM_011527547.1:c.448C=	XP_011525849.1:p.Gln150=
XM_005259441.4:c.310C=	XP_005259498.2:p.Gln104=
XM_011527545.3:c.*90C=	XP_011525847.1:n.*90C=
XM_011527546.2:c.475+203C=	XP_011525848.1:n.475+203C=
NM_001302961.2:c.310C=	NP_001289890.1:p.Gln104=
NR_126566.2:n.584C=
NM_004917.5:c.595C= MANE Select	NP_004908.4:p.Gln199=