Canonical Allele Identifier: CA2341138474

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908824T= , CM000681.2:g.50908824T=	GRCh38
NC_000019.9:g.51412080T= , CM000681.1:g.51412080T=	GRCh37
NC_000019.8:g.56103892T=	NCBI36
NG_012154.2:g.6915A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.230A= MANE Select	ENSP00000326159.1:p.Tyr77=
ENST00000324041.5:c.230A=	ENSP00000326159.1:p.Tyr77=
ENST00000431178.2:c.83A=	ENSP00000399448.2:p.Tyr28=
ENST00000593885.1:c.-56A=	ENSP00000469769.1:n.-56A=
ENST00000596876.1:n.149A=
ENST00000598305.5:c.-56A=	ENSP00000469963.1:n.-56A=
ENST00000599865.5:n.83A=
ENST00000602148.1:c.242A=	ENSP00000472091.1:n.242A=
NM_001302961.1:c.-56A=	NP_001289890.1:n.-56A=
NM_004917.4:c.230A=	NP_004908.4:p.Tyr77=
NR_126566.1:n.223A=
XM_005259441.3:c.-56A=	XP_005259498.2:n.-56A=
XM_011527545.1:c.230A=	XP_011525847.1:p.Tyr77=
XM_011527546.1:c.230A=	XP_011525848.1:p.Tyr77=
XM_011527547.1:c.83A=	XP_011525849.1:p.Tyr28=
XM_005259441.4:c.-56A=	XP_005259498.2:n.-56A=
XM_011527545.3:c.230A=	XP_011525847.1:p.Tyr77=
XM_011527546.2:c.230A=	XP_011525848.1:p.Tyr77=
NM_001302961.2:c.-56A=	NP_001289890.1:n.-56A=
NR_126566.2:n.223A=
NM_004917.5:c.230A= MANE Select	NP_004908.4:p.Tyr77=