Canonical Allele Identifier: CA2341138282

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908455C= , CM000681.2:g.50908455C=	GRCh38
NC_000019.9:g.51411711C= , CM000681.1:g.51411711C=	GRCh37
NC_000019.8:g.56103523C=	NCBI36
NG_012154.2:g.7284G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.516G= MANE Select	ENSP00000326159.1:p.Val172=
ENST00000324041.5:c.516G=	ENSP00000326159.1:p.Val172=
ENST00000431178.2:c.328+124G=	ENSP00000399448.2:n.328+124G=
ENST00000593885.1:c.*11G=	ENSP00000469769.1:n.*11G=
ENST00000596876.1:n.518G=
ENST00000598305.5:c.*11G=	ENSP00000469963.1:n.*11G=
ENST00000599865.5:n.452G=
ENST00000602148.1:c.528G=	ENSP00000472091.1:n.528G=
NM_001302961.1:c.231G=	NP_001289890.1:p.Val77=
NM_004917.4:c.516G=	NP_004908.4:p.Val172=
NR_126566.1:n.505G=
XM_005259441.3:c.231G=	XP_005259498.2:p.Val77=
XM_011527545.1:c.*11G=	XP_011525847.1:n.*11G=
XM_011527546.1:c.475+124G=	XP_011525848.1:n.475+124G=
XM_011527547.1:c.369G=	XP_011525849.1:p.Val123=
XM_005259441.4:c.231G=	XP_005259498.2:p.Val77=
XM_011527545.3:c.*11G=	XP_011525847.1:n.*11G=
XM_011527546.2:c.475+124G=	XP_011525848.1:n.475+124G=
NM_001302961.2:c.231G=	NP_001289890.1:p.Val77=
NR_126566.2:n.505G=
NM_004917.5:c.516G= MANE Select	NP_004908.4:p.Val172=