Canonical Allele Identifier: CA2341138279

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908441A= , CM000681.2:g.50908441A=	GRCh38
NC_000019.9:g.51411697A= , CM000681.1:g.51411697A=	GRCh37
NC_000019.8:g.56103509A=	NCBI36
NG_012154.2:g.7298T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.530T= MANE Select	ENSP00000326159.1:p.Val177=
ENST00000324041.5:c.530T=	ENSP00000326159.1:p.Val177=
ENST00000431178.2:c.328+138T=	ENSP00000399448.2:n.328+138T=
ENST00000593885.1:c.*25T=	ENSP00000469769.1:n.*25T=
ENST00000596876.1:n.532T=
ENST00000598305.5:c.*25T=	ENSP00000469963.1:n.*25T=
ENST00000599865.5:n.466T=
ENST00000602148.1:c.542T=	ENSP00000472091.1:n.542T=
NM_001302961.1:c.245T=	NP_001289890.1:p.Val82=
NM_004917.4:c.530T=	NP_004908.4:p.Val177=
NR_126566.1:n.519T=
XM_005259441.3:c.245T=	XP_005259498.2:p.Val82=
XM_011527545.1:c.*25T=	XP_011525847.1:n.*25T=
XM_011527546.1:c.475+138T=	XP_011525848.1:n.475+138T=
XM_011527547.1:c.383T=	XP_011525849.1:p.Val128=
XM_005259441.4:c.245T=	XP_005259498.2:p.Val82=
XM_011527545.3:c.*25T=	XP_011525847.1:n.*25T=
XM_011527546.2:c.475+138T=	XP_011525848.1:n.475+138T=
NM_001302961.2:c.245T=	NP_001289890.1:p.Val82=
NR_126566.2:n.519T=
NM_004917.5:c.530T= MANE Select	NP_004908.4:p.Val177=