Canonical Allele Identifier: CA2341138372

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908621C= , CM000681.2:g.50908621C=	GRCh38
NC_000019.9:g.51411877C= , CM000681.1:g.51411877C=	GRCh37
NC_000019.8:g.56103689C=	NCBI36
NG_012154.2:g.7118G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.433G= MANE Select	ENSP00000326159.1:p.Gly145=
ENST00000324041.5:c.433G=	ENSP00000326159.1:p.Gly145=
ENST00000431178.2:c.286G=	ENSP00000399448.2:p.Gly96=
ENST00000593885.1:c.148G=	ENSP00000469769.1:p.Gly50=
ENST00000596876.1:n.352G=
ENST00000598305.5:c.148G=	ENSP00000469963.1:p.Gly50=
ENST00000599865.5:n.286G=
ENST00000602148.1:c.445G=	ENSP00000472091.1:n.445G=
NM_001302961.1:c.148G=	NP_001289890.1:p.Gly50=
NM_004917.4:c.433G=	NP_004908.4:p.Gly145=
NR_126566.1:n.426G=
XM_005259441.3:c.148G=	XP_005259498.2:p.Gly50=
XM_011527545.1:c.433G=	XP_011525847.1:p.Gly145=
XM_011527546.1:c.433G=	XP_011525848.1:p.Gly145=
XM_011527547.1:c.286G=	XP_011525849.1:p.Gly96=
XM_005259441.4:c.148G=	XP_005259498.2:p.Gly50=
XM_011527545.3:c.433G=	XP_011525847.1:p.Gly145=
XM_011527546.2:c.433G=	XP_011525848.1:p.Gly145=
NM_001302961.2:c.148G=	NP_001289890.1:p.Gly50=
NR_126566.2:n.426G=
NM_004917.5:c.433G= MANE Select	NP_004908.4:p.Gly145=