Canonical Allele Identifier: CA2341138413

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908702T= , CM000681.2:g.50908702T=	GRCh38
NC_000019.9:g.51411958T= , CM000681.1:g.51411958T=	GRCh37
NC_000019.8:g.56103770T=	NCBI36
NG_012154.2:g.7037A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.352A= MANE Select	ENSP00000326159.1:p.Met118=
ENST00000324041.5:c.352A=	ENSP00000326159.1:p.Met118=
ENST00000431178.2:c.205A=	ENSP00000399448.2:p.Met69=
ENST00000593885.1:c.67A=	ENSP00000469769.1:p.Met23=
ENST00000596876.1:n.271A=
ENST00000598305.5:c.67A=	ENSP00000469963.1:p.Met23=
ENST00000599865.5:n.205A=
ENST00000602148.1:c.364A=	ENSP00000472091.1:n.364A=
NM_001302961.1:c.67A=	NP_001289890.1:p.Met23=
NM_004917.4:c.352A=	NP_004908.4:p.Met118=
NR_126566.1:n.345A=
XM_005259441.3:c.67A=	XP_005259498.2:p.Met23=
XM_011527545.1:c.352A=	XP_011525847.1:p.Met118=
XM_011527546.1:c.352A=	XP_011525848.1:p.Met118=
XM_011527547.1:c.205A=	XP_011525849.1:p.Met69=
XM_005259441.4:c.67A=	XP_005259498.2:p.Met23=
XM_011527545.3:c.352A=	XP_011525847.1:p.Met118=
XM_011527546.2:c.352A=	XP_011525848.1:p.Met118=
NM_001302961.2:c.67A=	NP_001289890.1:p.Met23=
NR_126566.2:n.345A=
NM_004917.5:c.352A= MANE Select	NP_004908.4:p.Met118=