Canonical Allele Identifier: CA2341138271

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908422G= , CM000681.2:g.50908422G=	GRCh38
NC_000019.9:g.51411678G= , CM000681.1:g.51411678G=	GRCh37
NC_000019.8:g.56103490G=	NCBI36
NG_012154.2:g.7317C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.549C= MANE Select	ENSP00000326159.1:p.Asp183=
ENST00000324041.5:c.549C=	ENSP00000326159.1:p.Asp183=
ENST00000431178.2:c.328+157C=	ENSP00000399448.2:n.328+157C=
ENST00000593885.1:c.*44C=	ENSP00000469769.1:n.*44C=
ENST00000596876.1:n.551C=
ENST00000598305.5:c.*44C=	ENSP00000469963.1:n.*44C=
ENST00000599865.5:n.485C=
ENST00000602148.1:c.561C=	ENSP00000472091.1:n.561C=
NM_001302961.1:c.264C=	NP_001289890.1:p.Asp88=
NM_004917.4:c.549C=	NP_004908.4:p.Asp183=
NR_126566.1:n.538C=
XM_005259441.3:c.264C=	XP_005259498.2:p.Asp88=
XM_011527545.1:c.*44C=	XP_011525847.1:n.*44C=
XM_011527546.1:c.475+157C=	XP_011525848.1:n.475+157C=
XM_011527547.1:c.402C=	XP_011525849.1:p.Asp134=
XM_005259441.4:c.264C=	XP_005259498.2:p.Asp88=
XM_011527545.3:c.*44C=	XP_011525847.1:n.*44C=
XM_011527546.2:c.475+157C=	XP_011525848.1:n.475+157C=
NM_001302961.2:c.264C=	NP_001289890.1:p.Asp88=
NR_126566.2:n.538C=
NM_004917.5:c.549C= MANE Select	NP_004908.4:p.Asp183=