Canonical Allele Identifier: CA2341138308

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908511C= , CM000681.2:g.50908511C=	GRCh38
NC_000019.9:g.51411767C= , CM000681.1:g.51411767C=	GRCh37
NC_000019.8:g.56103579C=	NCBI36
NG_012154.2:g.7228G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000324041.6:c.476-16G= MANE Select	ENSP00000326159.1:n.476-16G=
ENST00000324041.5:c.476-16G=	ENSP00000326159.1:n.476-16G=
ENST00000431178.2:c.328+68G=	ENSP00000399448.2:n.328+68G=
ENST00000593885.1:c.191-20G=	ENSP00000469769.1:n.191-20G=
ENST00000596876.1:n.462G=
ENST00000598305.5:c.191-20G=	ENSP00000469963.1:n.191-20G=
ENST00000599865.5:n.396G=
ENST00000602148.1:c.488-16G=	ENSP00000472091.1:n.488-16G=
NM_001302961.1:c.191-16G=	NP_001289890.1:n.191-16G=
NM_004917.4:c.476-16G=	NP_004908.4:n.476-16G=
NR_126566.1:n.469-20G=
XM_005259441.3:c.191-16G=	XP_005259498.2:n.191-16G=
XM_011527545.1:c.476-20G=	XP_011525847.1:n.476-20G=
XM_011527546.1:c.475+68G=	XP_011525848.1:n.475+68G=
XM_011527547.1:c.329-16G=	XP_011525849.1:n.329-16G=
XM_005259441.4:c.191-16G=	XP_005259498.2:n.191-16G=
XM_011527545.3:c.476-20G=	XP_011525847.1:n.476-20G=
XM_011527546.2:c.475+68G=	XP_011525848.1:n.475+68G=
NM_001302961.2:c.191-16G=	NP_001289890.1:n.191-16G=
NR_126566.2:n.469-20G=
NM_004917.5:c.476-16G= MANE Select	NP_004908.4:n.476-16G=