Canonical Allele Identifier: CA2341138469

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908815C= , CM000681.2:g.50908815C=	GRCh38
NC_000019.9:g.51412071C= , CM000681.1:g.51412071C=	GRCh37
NC_000019.8:g.56103883C=	NCBI36
NG_012154.2:g.6924G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.239G= MANE Select	ENSP00000326159.1:p.Gly80=
ENST00000324041.5:c.239G=	ENSP00000326159.1:p.Gly80=
ENST00000431178.2:c.92G=	ENSP00000399448.2:p.Gly31=
ENST00000593885.1:c.-47G=	ENSP00000469769.1:n.-47G=
ENST00000596876.1:n.158G=
ENST00000598305.5:c.-47G=	ENSP00000469963.1:n.-47G=
ENST00000599865.5:n.92G=
ENST00000602148.1:c.251G=	ENSP00000472091.1:n.251G=
NM_001302961.1:c.-47G=	NP_001289890.1:n.-47G=
NM_004917.4:c.239G=	NP_004908.4:p.Gly80=
NR_126566.1:n.232G=
XM_005259441.3:c.-47G=	XP_005259498.2:n.-47G=
XM_011527545.1:c.239G=	XP_011525847.1:p.Gly80=
XM_011527546.1:c.239G=	XP_011525848.1:p.Gly80=
XM_011527547.1:c.92G=	XP_011525849.1:p.Gly31=
XM_005259441.4:c.-47G=	XP_005259498.2:n.-47G=
XM_011527545.3:c.239G=	XP_011525847.1:p.Gly80=
XM_011527546.2:c.239G=	XP_011525848.1:p.Gly80=
NM_001302961.2:c.-47G=	NP_001289890.1:n.-47G=
NR_126566.2:n.232G=
NM_004917.5:c.239G= MANE Select	NP_004908.4:p.Gly80=