Canonical Allele Identifier: CA2341138245

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908364A= , CM000681.2:g.50908364A=	GRCh38
NC_000019.9:g.51411620A= , CM000681.1:g.51411620A=	GRCh37
NC_000019.8:g.56103432A=	NCBI36
NG_012154.2:g.7375T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.607T= MANE Select	ENSP00000326159.1:p.Cys203=
ENST00000324041.5:c.607T=	ENSP00000326159.1:p.Cys203=
ENST00000431178.2:c.328+215T=	ENSP00000399448.2:n.328+215T=
ENST00000593885.1:c.*102T=	ENSP00000469769.1:n.*102T=
ENST00000596876.1:n.609T=
ENST00000598305.5:c.*102T=	ENSP00000469963.1:n.*102T=
ENST00000599865.5:n.543T=
ENST00000602148.1:c.619T=	ENSP00000472091.1:n.619T=
NM_001302961.1:c.322T=	NP_001289890.1:p.Cys108=
NM_004917.4:c.607T=	NP_004908.4:p.Cys203=
NR_126566.1:n.596T=
XM_005259441.3:c.322T=	XP_005259498.2:p.Cys108=
XM_011527546.1:c.475+215T=	XP_011525848.1:n.475+215T=
XM_011527547.1:c.460T=	XP_011525849.1:p.Cys154=
XM_005259441.4:c.322T=	XP_005259498.2:p.Cys108=
XM_011527546.2:c.475+215T=	XP_011525848.1:n.475+215T=
NM_001302961.2:c.322T=	NP_001289890.1:p.Cys108=
NR_126566.2:n.596T=
NM_004917.5:c.607T= MANE Select	NP_004908.4:p.Cys203=