Canonical Allele Identifier: CA2341138277

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908437G= , CM000681.2:g.50908437G=	GRCh38
NC_000019.9:g.51411693G= , CM000681.1:g.51411693G=	GRCh37
NC_000019.8:g.56103505G=	NCBI36
NG_012154.2:g.7302C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.534C= MANE Select	ENSP00000326159.1:p.Cys178=
ENST00000324041.5:c.534C=	ENSP00000326159.1:p.Cys178=
ENST00000431178.2:c.328+142C=	ENSP00000399448.2:n.328+142C=
ENST00000593885.1:c.*29C=	ENSP00000469769.1:n.*29C=
ENST00000596876.1:n.536C=
ENST00000598305.5:c.*29C=	ENSP00000469963.1:n.*29C=
ENST00000599865.5:n.470C=
ENST00000602148.1:c.546C=	ENSP00000472091.1:n.546C=
NM_001302961.1:c.249C=	NP_001289890.1:p.Cys83=
NM_004917.4:c.534C=	NP_004908.4:p.Cys178=
NR_126566.1:n.523C=
XM_005259441.3:c.249C=	XP_005259498.2:p.Cys83=
XM_011527545.1:c.*29C=	XP_011525847.1:n.*29C=
XM_011527546.1:c.475+142C=	XP_011525848.1:n.475+142C=
XM_011527547.1:c.387C=	XP_011525849.1:p.Cys129=
XM_005259441.4:c.249C=	XP_005259498.2:p.Cys83=
XM_011527545.3:c.*29C=	XP_011525847.1:n.*29C=
XM_011527546.2:c.475+142C=	XP_011525848.1:n.475+142C=
NM_001302961.2:c.249C=	NP_001289890.1:p.Cys83=
NR_126566.2:n.523C=
NM_004917.5:c.534C= MANE Select	NP_004908.4:p.Cys178=