Canonical Allele Identifier: CA2341138270

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908419C= , CM000681.2:g.50908419C=	GRCh38
NC_000019.9:g.51411675C= , CM000681.1:g.51411675C=	GRCh37
NC_000019.8:g.56103487C=	NCBI36
NG_012154.2:g.7320G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.552G= MANE Select	ENSP00000326159.1:p.Pro184=
ENST00000324041.5:c.552G=	ENSP00000326159.1:p.Pro184=
ENST00000431178.2:c.328+160G=	ENSP00000399448.2:n.328+160G=
ENST00000593885.1:c.*47G=	ENSP00000469769.1:n.*47G=
ENST00000596876.1:n.554G=
ENST00000598305.5:c.*47G=	ENSP00000469963.1:n.*47G=
ENST00000599865.5:n.488G=
ENST00000602148.1:c.564G=	ENSP00000472091.1:n.564G=
NM_001302961.1:c.267G=	NP_001289890.1:p.Pro89=
NM_004917.4:c.552G=	NP_004908.4:p.Pro184=
NR_126566.1:n.541G=
XM_005259441.3:c.267G=	XP_005259498.2:p.Pro89=
XM_011527545.1:c.*47G=	XP_011525847.1:n.*47G=
XM_011527546.1:c.475+160G=	XP_011525848.1:n.475+160G=
XM_011527547.1:c.405G=	XP_011525849.1:p.Pro135=
XM_005259441.4:c.267G=	XP_005259498.2:p.Pro89=
XM_011527545.3:c.*47G=	XP_011525847.1:n.*47G=
XM_011527546.2:c.475+160G=	XP_011525848.1:n.475+160G=
NM_001302961.2:c.267G=	NP_001289890.1:p.Pro89=
NR_126566.2:n.541G=
NM_004917.5:c.552G= MANE Select	NP_004908.4:p.Pro184=