Canonical Allele Identifier: CA2341138394

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908661G= , CM000681.2:g.50908661G=	GRCh38
NC_000019.9:g.51411917G= , CM000681.1:g.51411917G=	GRCh37
NC_000019.8:g.56103729G=	NCBI36
NG_012154.2:g.7078C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.393C= MANE Select	ENSP00000326159.1:p.Thr131=
ENST00000324041.5:c.393C=	ENSP00000326159.1:p.Thr131=
ENST00000431178.2:c.246C=	ENSP00000399448.2:p.Thr82=
ENST00000593885.1:c.108C=	ENSP00000469769.1:p.Thr36=
ENST00000596876.1:n.312C=
ENST00000598305.5:c.108C=	ENSP00000469963.1:p.Thr36=
ENST00000599865.5:n.246C=
ENST00000602148.1:c.405C=	ENSP00000472091.1:n.405C=
NM_001302961.1:c.108C=	NP_001289890.1:p.Thr36=
NM_004917.4:c.393C=	NP_004908.4:p.Thr131=
NR_126566.1:n.386C=
XM_005259441.3:c.108C=	XP_005259498.2:p.Thr36=
XM_011527545.1:c.393C=	XP_011525847.1:p.Thr131=
XM_011527546.1:c.393C=	XP_011525848.1:p.Thr131=
XM_011527547.1:c.246C=	XP_011525849.1:p.Thr82=
XM_005259441.4:c.108C=	XP_005259498.2:p.Thr36=
XM_011527545.3:c.393C=	XP_011525847.1:p.Thr131=
XM_011527546.2:c.393C=	XP_011525848.1:p.Thr131=
NM_001302961.2:c.108C=	NP_001289890.1:p.Thr36=
NR_126566.2:n.386C=
NM_004917.5:c.393C= MANE Select	NP_004908.4:p.Thr131=