Canonical Allele Identifier: CA2341138114

Gene: KLK4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908133G= , CM000681.2:g.50908133G=	GRCh38
NC_000019.9:g.51411389G= , CM000681.1:g.51411389G=	GRCh37
NC_000019.8:g.56103201G=	NCBI36
NG_012154.2:g.7606C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.612+226C= MANE Select	ENSP00000326159.1:n.612+226C=
ENST00000324041.5:c.612+226C=	ENSP00000326159.1:n.612+226C=
ENST00000431178.2:c.328+446C=	ENSP00000399448.2:n.328+446C=
ENST00000593885.1:c.*107+226C=	ENSP00000469769.1:n.*107+226C=
ENST00000596876.1:n.840C=
ENST00000598305.5:c.*107+226C=	ENSP00000469963.1:n.*107+226C=
ENST00000599865.5:n.548+226C=
ENST00000602148.1:c.624+226C=	ENSP00000472091.1:n.624+226C=
NM_001302961.1:c.327+226C=	NP_001289890.1:n.327+226C=
NM_004917.4:c.612+226C=	NP_004908.4:n.612+226C=
NR_126566.1:n.601+226C=
XM_005259441.3:c.327+226C=	XP_005259498.2:n.327+226C=
XM_011527546.1:c.475+446C=	XP_011525848.1:n.475+446C=
XM_011527547.1:c.465+226C=	XP_011525849.1:n.465+226C=
XM_005259441.4:c.327+226C=	XP_005259498.2:n.327+226C=
XM_011527546.2:c.475+446C=	XP_011525848.1:n.475+446C=
NM_001302961.2:c.327+226C=	NP_001289890.1:n.327+226C=
NR_126566.2:n.601+226C=
NM_004917.5:c.612+226C= MANE Select	NP_004908.4:n.612+226C=