Canonical Allele Identifier: CA2341138397

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908669A= , CM000681.2:g.50908669A=	GRCh38
NC_000019.9:g.51411925A= , CM000681.1:g.51411925A=	GRCh37
NC_000019.8:g.56103737A=	NCBI36
NG_012154.2:g.7070T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.385T= MANE Select	ENSP00000326159.1:p.Ser129=
ENST00000324041.5:c.385T=	ENSP00000326159.1:p.Ser129=
ENST00000431178.2:c.238T=	ENSP00000399448.2:p.Ser80=
ENST00000593885.1:c.100T=	ENSP00000469769.1:p.Ser34=
ENST00000596876.1:n.304T=
ENST00000598305.5:c.100T=	ENSP00000469963.1:p.Ser34=
ENST00000599865.5:n.238T=
ENST00000602148.1:c.397T=	ENSP00000472091.1:n.397T=
NM_001302961.1:c.100T=	NP_001289890.1:p.Ser34=
NM_004917.4:c.385T=	NP_004908.4:p.Ser129=
NR_126566.1:n.378T=
XM_005259441.3:c.100T=	XP_005259498.2:p.Ser34=
XM_011527545.1:c.385T=	XP_011525847.1:p.Ser129=
XM_011527546.1:c.385T=	XP_011525848.1:p.Ser129=
XM_011527547.1:c.238T=	XP_011525849.1:p.Ser80=
XM_005259441.4:c.100T=	XP_005259498.2:p.Ser34=
XM_011527545.3:c.385T=	XP_011525847.1:p.Ser129=
XM_011527546.2:c.385T=	XP_011525848.1:p.Ser129=
NM_001302961.2:c.100T=	NP_001289890.1:p.Ser34=
NR_126566.2:n.378T=
NM_004917.5:c.385T= MANE Select	NP_004908.4:p.Ser129=