Canonical Allele Identifier: CA2341115595

Gene: KLK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860123_50860125delinsCCT , CM000681.2:g.50860123_50860125delinsCCT	GRCh38
NC_000019.9:g.51363379_51363381delinsCCT , CM000681.1:g.51363379_51363381delinsCCT	GRCh37
NC_000019.8:g.56055191_56055193delinsCCT	NCBI36
NG_011653.1:g.10209_10211delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.782_784delinsCCT MANE Select	ENSP00000314151.1:p.Pro261=
ENST00000326003.6:c.782_784delinsCCT	ENSP00000314151.1:p.Pro261=
ENST00000360617.7:c.1224_1226delinsCCT	ENSP00000353829.2:n.1224_1226delinsCCT
ENST00000422986.6:c.*438_*440delinsCCT	ENSP00000393628.2:n.*438_*440delinsCCT
ENST00000595392.5:c.*283_*285delinsCCT	ENSP00000468912.1:n.*283_*285delinsCCT
ENST00000595952.5:c.653_655delinsCCT	ENSP00000471155.1:p.Pro218=
ENST00000596333.1:n.960_962delinsCCT
ENST00000598145.1:c.784_786delinsCCT
ENST00000601349.5:n.2061_2063delinsCCT
ENST00000601812.1:n.1214_1216delinsCCT
ENST00000617027.4:c.659_661delinsCCT	ENSP00000483513.1:p.Pro220=
NM_001030047.1:c.*507_*509delinsCCT	NP_001025218.1:n.*507_*509delinsCCT
NM_001030048.1:c.653_655delinsCCT	NP_001025219.1:p.Pro218=
NM_001648.2:c.782_784delinsCCT MANE Select	NP_001639.1:p.Pro261=
XM_011526923.1:c.800_802delinsCCT	XP_011525225.1:p.Pro267=
XR_935817.1:n.1324+869_1324+871delinsCCT