Canonical Allele Identifier: CA2341138248

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908371C= , CM000681.2:g.50908371C=	GRCh38
NC_000019.9:g.51411627C= , CM000681.1:g.51411627C=	GRCh37
NC_000019.8:g.56103439C=	NCBI36
NG_012154.2:g.7368G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.600G= MANE Select	ENSP00000326159.1:p.Lys200=
ENST00000324041.5:c.600G=	ENSP00000326159.1:p.Lys200=
ENST00000431178.2:c.328+208G=	ENSP00000399448.2:n.328+208G=
ENST00000593885.1:c.*95G=	ENSP00000469769.1:n.*95G=
ENST00000596876.1:n.602G=
ENST00000598305.5:c.*95G=	ENSP00000469963.1:n.*95G=
ENST00000599865.5:n.536G=
ENST00000602148.1:c.612G=	ENSP00000472091.1:n.612G=
NM_001302961.1:c.315G=	NP_001289890.1:p.Lys105=
NM_004917.4:c.600G=	NP_004908.4:p.Lys200=
NR_126566.1:n.589G=
XM_005259441.3:c.315G=	XP_005259498.2:p.Lys105=
XM_011527546.1:c.475+208G=	XP_011525848.1:n.475+208G=
XM_011527547.1:c.453G=	XP_011525849.1:p.Lys151=
XM_005259441.4:c.315G=	XP_005259498.2:p.Lys105=
XM_011527545.3:c.*95G=	XP_011525847.1:n.*95G=
XM_011527546.2:c.475+208G=	XP_011525848.1:n.475+208G=
NM_001302961.2:c.315G=	NP_001289890.1:p.Lys105=
NR_126566.2:n.589G=
NM_004917.5:c.600G= MANE Select	NP_004908.4:p.Lys200=