Canonical Allele Identifier: CA2341138288

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908463C= , CM000681.2:g.50908463C=	GRCh38
NC_000019.9:g.51411719C= , CM000681.1:g.51411719C=	GRCh37
NC_000019.8:g.56103531C=	NCBI36
NG_012154.2:g.7276G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.508G= MANE Select	ENSP00000326159.1:p.Val170=
ENST00000324041.5:c.508G=	ENSP00000326159.1:p.Val170=
ENST00000431178.2:c.328+116G=	ENSP00000399448.2:n.328+116G=
ENST00000593885.1:c.*3G=	ENSP00000469769.1:n.*3G=
ENST00000596876.1:n.510G=
ENST00000598305.5:c.*3G=	ENSP00000469963.1:n.*3G=
ENST00000599865.5:n.444G=
ENST00000602148.1:c.520G=	ENSP00000472091.1:n.520G=
NM_001302961.1:c.223G=	NP_001289890.1:p.Val75=
NM_004917.4:c.508G=	NP_004908.4:p.Val170=
NR_126566.1:n.497G=
XM_005259441.3:c.223G=	XP_005259498.2:p.Val75=
XM_011527545.1:c.*3G=	XP_011525847.1:n.*3G=
XM_011527546.1:c.475+116G=	XP_011525848.1:n.475+116G=
XM_011527547.1:c.361G=	XP_011525849.1:p.Val121=
XM_005259441.4:c.223G=	XP_005259498.2:p.Val75=
XM_011527545.3:c.*3G=	XP_011525847.1:n.*3G=
XM_011527546.2:c.475+116G=	XP_011525848.1:n.475+116G=
NM_001302961.2:c.223G=	NP_001289890.1:p.Val75=
NR_126566.2:n.497G=
NM_004917.5:c.508G= MANE Select	NP_004908.4:p.Val170=