Canonical Allele Identifier: CA2341138389

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908653C= , CM000681.2:g.50908653C=	GRCh38
NC_000019.9:g.51411909C= , CM000681.1:g.51411909C=	GRCh37
NC_000019.8:g.56103721C=	NCBI36
NG_012154.2:g.7086G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.401G= MANE Select	ENSP00000326159.1:p.Ser134=
ENST00000324041.5:c.401G=	ENSP00000326159.1:p.Ser134=
ENST00000431178.2:c.254G=	ENSP00000399448.2:p.Ser85=
ENST00000593885.1:c.116G=	ENSP00000469769.1:p.Ser39=
ENST00000596876.1:n.320G=
ENST00000598305.5:c.116G=	ENSP00000469963.1:p.Ser39=
ENST00000599865.5:n.254G=
ENST00000602148.1:c.413G=	ENSP00000472091.1:n.413G=
NM_001302961.1:c.116G=	NP_001289890.1:p.Ser39=
NM_004917.4:c.401G=	NP_004908.4:p.Ser134=
NR_126566.1:n.394G=
XM_005259441.3:c.116G=	XP_005259498.2:p.Ser39=
XM_011527545.1:c.401G=	XP_011525847.1:p.Ser134=
XM_011527546.1:c.401G=	XP_011525848.1:p.Ser134=
XM_011527547.1:c.254G=	XP_011525849.1:p.Ser85=
XM_005259441.4:c.116G=	XP_005259498.2:p.Ser39=
XM_011527545.3:c.401G=	XP_011525847.1:p.Ser134=
XM_011527546.2:c.401G=	XP_011525848.1:p.Ser134=
NM_001302961.2:c.116G=	NP_001289890.1:p.Ser39=
NR_126566.2:n.394G=
NM_004917.5:c.401G= MANE Select	NP_004908.4:p.Ser134=