Canonical Allele Identifier: CA2341138283

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908457C= , CM000681.2:g.50908457C=	GRCh38
NC_000019.9:g.51411713C= , CM000681.1:g.51411713C=	GRCh37
NC_000019.8:g.56103525C=	NCBI36
NG_012154.2:g.7282G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.514G= MANE Select	ENSP00000326159.1:p.Val172=
ENST00000324041.5:c.514G=	ENSP00000326159.1:p.Val172=
ENST00000431178.2:c.328+122G=	ENSP00000399448.2:n.328+122G=
ENST00000593885.1:c.*9G=	ENSP00000469769.1:n.*9G=
ENST00000596876.1:n.516G=
ENST00000598305.5:c.*9G=	ENSP00000469963.1:n.*9G=
ENST00000599865.5:n.450G=
ENST00000602148.1:c.526G=	ENSP00000472091.1:n.526G=
NM_001302961.1:c.229G=	NP_001289890.1:p.Val77=
NM_004917.4:c.514G=	NP_004908.4:p.Val172=
NR_126566.1:n.503G=
XM_005259441.3:c.229G=	XP_005259498.2:p.Val77=
XM_011527545.1:c.*9G=	XP_011525847.1:n.*9G=
XM_011527546.1:c.475+122G=	XP_011525848.1:n.475+122G=
XM_011527547.1:c.367G=	XP_011525849.1:p.Val123=
XM_005259441.4:c.229G=	XP_005259498.2:p.Val77=
XM_011527545.3:c.*9G=	XP_011525847.1:n.*9G=
XM_011527546.2:c.475+122G=	XP_011525848.1:n.475+122G=
NM_001302961.2:c.229G=	NP_001289890.1:p.Val77=
NR_126566.2:n.503G=
NM_004917.5:c.514G= MANE Select	NP_004908.4:p.Val172=