Canonical Allele Identifier: CA2341138418

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908716A= , CM000681.2:g.50908716A=	GRCh38
NC_000019.9:g.51411972A= , CM000681.1:g.51411972A=	GRCh37
NC_000019.8:g.56103784A=	NCBI36
NG_012154.2:g.7023T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000324041.6:c.338T= MANE Select	ENSP00000326159.1:p.Leu113=
ENST00000324041.5:c.338T=	ENSP00000326159.1:p.Leu113=
ENST00000431178.2:c.191T=	ENSP00000399448.2:p.Leu64=
ENST00000593885.1:c.53T=	ENSP00000469769.1:p.Leu18=
ENST00000596876.1:n.257T=
ENST00000598305.5:c.53T=	ENSP00000469963.1:p.Leu18=
ENST00000599865.5:n.191T=
ENST00000602148.1:c.350T=	ENSP00000472091.1:n.350T=
NM_001302961.1:c.53T=	NP_001289890.1:p.Leu18=
NM_004917.4:c.338T=	NP_004908.4:p.Leu113=
NR_126566.1:n.331T=
XM_005259441.3:c.53T=	XP_005259498.2:p.Leu18=
XM_011527545.1:c.338T=	XP_011525847.1:p.Leu113=
XM_011527546.1:c.338T=	XP_011525848.1:p.Leu113=
XM_011527547.1:c.191T=	XP_011525849.1:p.Leu64=
XM_005259441.4:c.53T=	XP_005259498.2:p.Leu18=
XM_011527545.3:c.338T=	XP_011525847.1:p.Leu113=
XM_011527546.2:c.338T=	XP_011525848.1:p.Leu113=
NM_001302961.2:c.53T=	NP_001289890.1:p.Leu18=
NR_126566.2:n.331T=
NM_004917.5:c.338T= MANE Select	NP_004908.4:p.Leu113=