Canonical Allele Identifier: CA2341138330

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908537A= , CM000681.2:g.50908537A=	GRCh38
NC_000019.9:g.51411793A= , CM000681.1:g.51411793A=	GRCh37
NC_000019.8:g.56103605A=	NCBI36
NG_012154.2:g.7202T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.476-42T= MANE Select	ENSP00000326159.1:n.476-42T=
ENST00000324041.5:c.476-42T=	ENSP00000326159.1:n.476-42T=
ENST00000431178.2:c.328+42T=	ENSP00000399448.2:n.328+42T=
ENST00000593885.1:c.190+42T=	ENSP00000469769.1:n.190+42T=
ENST00000596876.1:n.436T=
ENST00000598305.5:c.190+42T=	ENSP00000469963.1:n.190+42T=
ENST00000599865.5:n.370T=
ENST00000602148.1:c.488-42T=	ENSP00000472091.1:n.488-42T=
NM_001302961.1:c.191-42T=	NP_001289890.1:n.191-42T=
NM_004917.4:c.476-42T=	NP_004908.4:n.476-42T=
NR_126566.1:n.468+42T=
XM_005259441.3:c.191-42T=	XP_005259498.2:n.191-42T=
XM_011527545.1:c.475+42T=	XP_011525847.1:n.475+42T=
XM_011527546.1:c.475+42T=	XP_011525848.1:n.475+42T=
XM_011527547.1:c.329-42T=	XP_011525849.1:n.329-42T=
XM_005259441.4:c.191-42T=	XP_005259498.2:n.191-42T=
XM_011527545.3:c.475+42T=	XP_011525847.1:n.475+42T=
XM_011527546.2:c.475+42T=	XP_011525848.1:n.475+42T=
NM_001302961.2:c.191-42T=	NP_001289890.1:n.191-42T=
NR_126566.2:n.468+42T=
NM_004917.5:c.476-42T= MANE Select	NP_004908.4:n.476-42T=