Canonical Allele Identifier: CA2341138376

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908624C= , CM000681.2:g.50908624C=	GRCh38
NC_000019.9:g.51411880C= , CM000681.1:g.51411880C=	GRCh37
NC_000019.8:g.56103692C=	NCBI36
NG_012154.2:g.7115G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.430G= MANE Select	ENSP00000326159.1:p.Ala144=
ENST00000324041.5:c.430G=	ENSP00000326159.1:p.Ala144=
ENST00000431178.2:c.283G=	ENSP00000399448.2:p.Ala95=
ENST00000593885.1:c.145G=	ENSP00000469769.1:p.Ala49=
ENST00000596876.1:n.349G=
ENST00000598305.5:c.145G=	ENSP00000469963.1:p.Ala49=
ENST00000599865.5:n.283G=
ENST00000602148.1:c.442G=	ENSP00000472091.1:n.442G=
NM_001302961.1:c.145G=	NP_001289890.1:p.Ala49=
NM_004917.4:c.430G=	NP_004908.4:p.Ala144=
NR_126566.1:n.423G=
XM_005259441.3:c.145G=	XP_005259498.2:p.Ala49=
XM_011527545.1:c.430G=	XP_011525847.1:p.Ala144=
XM_011527546.1:c.430G=	XP_011525848.1:p.Ala144=
XM_011527547.1:c.283G=	XP_011525849.1:p.Ala95=
XM_005259441.4:c.145G=	XP_005259498.2:p.Ala49=
XM_011527545.3:c.430G=	XP_011525847.1:p.Ala144=
XM_011527546.2:c.430G=	XP_011525848.1:p.Ala144=
NM_001302961.2:c.145G=	NP_001289890.1:p.Ala49=
NR_126566.2:n.423G=
NM_004917.5:c.430G= MANE Select	NP_004908.4:p.Ala144=