Canonical Allele Identifier: CA2341138409

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908692T= , CM000681.2:g.50908692T=	GRCh38
NC_000019.9:g.51411948T= , CM000681.1:g.51411948T=	GRCh37
NC_000019.8:g.56103760T=	NCBI36
NG_012154.2:g.7047A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.362A= MANE Select	ENSP00000326159.1:p.Lys121=
ENST00000324041.5:c.362A=	ENSP00000326159.1:p.Lys121=
ENST00000431178.2:c.215A=	ENSP00000399448.2:p.Lys72=
ENST00000593885.1:c.77A=	ENSP00000469769.1:p.Lys26=
ENST00000596876.1:n.281A=
ENST00000598305.5:c.77A=	ENSP00000469963.1:p.Lys26=
ENST00000599865.5:n.215A=
ENST00000602148.1:c.374A=	ENSP00000472091.1:n.374A=
NM_001302961.1:c.77A=	NP_001289890.1:p.Lys26=
NM_004917.4:c.362A=	NP_004908.4:p.Lys121=
NR_126566.1:n.355A=
XM_005259441.3:c.77A=	XP_005259498.2:p.Lys26=
XM_011527545.1:c.362A=	XP_011525847.1:p.Lys121=
XM_011527546.1:c.362A=	XP_011525848.1:p.Lys121=
XM_011527547.1:c.215A=	XP_011525849.1:p.Lys72=
XM_005259441.4:c.77A=	XP_005259498.2:p.Lys26=
XM_011527545.3:c.362A=	XP_011525847.1:p.Lys121=
XM_011527546.2:c.362A=	XP_011525848.1:p.Lys121=
NM_001302961.2:c.77A=	NP_001289890.1:p.Lys26=
NR_126566.2:n.355A=
NM_004917.5:c.362A= MANE Select	NP_004908.4:p.Lys121=