Canonical Allele Identifier: CA2341138443

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908767A= , CM000681.2:g.50908767A=	GRCh38
NC_000019.9:g.51412023A= , CM000681.1:g.51412023A=	GRCh37
NC_000019.8:g.56103835A=	NCBI36
NG_012154.2:g.6972T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.287T= MANE Select	ENSP00000326159.1:p.Met96=
ENST00000324041.5:c.287T=	ENSP00000326159.1:p.Met96=
ENST00000431178.2:c.140T=	ENSP00000399448.2:p.Met47=
ENST00000593885.1:c.2T=	ENSP00000469769.1:p.Met1=
ENST00000596876.1:n.206T=
ENST00000598305.5:c.2T=	ENSP00000469963.1:p.Met1=
ENST00000599865.5:n.140T=
ENST00000602148.1:c.299T=	ENSP00000472091.1:n.299T=
NM_001302961.1:c.2T=	NP_001289890.1:p.Met1=
NM_004917.4:c.287T=	NP_004908.4:p.Met96=
NR_126566.1:n.280T=
XM_005259441.3:c.2T=	XP_005259498.2:p.Met1=
XM_011527545.1:c.287T=	XP_011525847.1:p.Met96=
XM_011527546.1:c.287T=	XP_011525848.1:p.Met96=
XM_011527547.1:c.140T=	XP_011525849.1:p.Met47=
XM_005259441.4:c.2T=	XP_005259498.2:p.Met1=
XM_011527545.3:c.287T=	XP_011525847.1:p.Met96=
XM_011527546.2:c.287T=	XP_011525848.1:p.Met96=
NM_001302961.2:c.2T=	NP_001289890.1:p.Met1=
NR_126566.2:n.280T=
NM_004917.5:c.287T= MANE Select	NP_004908.4:p.Met96=