Canonical Allele Identifier: CA2341115598

Gene: KLK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860124_50860125delinsCT , CM000681.2:g.50860124_50860125delinsCT	GRCh38
NC_000019.9:g.51363380_51363381delinsCT , CM000681.1:g.51363380_51363381delinsCT	GRCh37
NC_000019.8:g.56055192_56055193delinsCT	NCBI36
NG_011653.1:g.10210_10211delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.783_784delinsCT MANE Select	ENSP00000314151.1:p.Pro261=
ENST00000326003.6:c.783_784delinsCT	ENSP00000314151.1:p.Pro261=
ENST00000360617.7:c.1225_1226delinsCT	ENSP00000353829.2:n.1225_1226delinsCT
ENST00000422986.6:c.*439_*440delinsCT	ENSP00000393628.2:n.*439_*440delinsCT
ENST00000595392.5:c.*284_*285delinsCT	ENSP00000468912.1:n.*284_*285delinsCT
ENST00000595952.5:c.654_655delinsCT	ENSP00000471155.1:p.Pro218=
ENST00000596333.1:n.961_962delinsCT
ENST00000598145.1:c.785_786delinsCT
ENST00000601349.5:n.2062_2063delinsCT
ENST00000601812.1:n.1215_1216delinsCT
ENST00000617027.4:c.660_661delinsCT	ENSP00000483513.1:p.Pro220=
NM_001030047.1:c.*508_*509delinsCT	NP_001025218.1:n.*508_*509delinsCT
NM_001030048.1:c.654_655delinsCT	NP_001025219.1:p.Pro218=
NM_001648.2:c.783_784delinsCT MANE Select	NP_001639.1:p.Pro261=
XM_011526923.1:c.801_802delinsCT	XP_011525225.1:p.Pro267=
XR_935817.1:n.1324+870_1324+871delinsCT