Canonical Allele Identifier: CA2341138296

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908482G= , CM000681.2:g.50908482G=	GRCh38
NC_000019.9:g.51411738G= , CM000681.1:g.51411738G=	GRCh37
NC_000019.8:g.56103550G=	NCBI36
NG_012154.2:g.7257C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.489C= MANE Select	ENSP00000326159.1:p.Thr163=
ENST00000324041.5:c.489C=	ENSP00000326159.1:p.Thr163=
ENST00000431178.2:c.328+97C=	ENSP00000399448.2:n.328+97C=
ENST00000593885.1:c.200C=	ENSP00000469769.1:p.Pro67=
ENST00000596876.1:n.491C=
ENST00000598305.5:c.200C=	ENSP00000469963.1:p.Pro67=
ENST00000599865.5:n.425C=
ENST00000602148.1:c.501C=	ENSP00000472091.1:n.501C=
NM_001302961.1:c.204C=	NP_001289890.1:p.Thr68=
NM_004917.4:c.489C=	NP_004908.4:p.Thr163=
NR_126566.1:n.478C=
XM_005259441.3:c.204C=	XP_005259498.2:p.Thr68=
XM_011527545.1:c.485C=	XP_011525847.1:p.Pro162=
XM_011527546.1:c.475+97C=	XP_011525848.1:n.475+97C=
XM_011527547.1:c.342C=	XP_011525849.1:p.Thr114=
XM_005259441.4:c.204C=	XP_005259498.2:p.Thr68=
XM_011527545.3:c.485C=	XP_011525847.1:p.Pro162=
XM_011527546.2:c.475+97C=	XP_011525848.1:n.475+97C=
NM_001302961.2:c.204C=	NP_001289890.1:p.Thr68=
NR_126566.2:n.478C=
NM_004917.5:c.489C= MANE Select	NP_004908.4:p.Thr163=