Canonical Allele Identifier: CA2341115607

Gene: KLK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860134_50860135delinsCT , CM000681.2:g.50860134_50860135delinsCT	GRCh38
NC_000019.9:g.51363390_51363391delinsCT , CM000681.1:g.51363390_51363391delinsCT	GRCh37
NC_000019.8:g.56055202_56055203delinsCT	NCBI36
NG_011653.1:g.10220_10221delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.*7_*8delinsCT MANE Select	ENSP00000314151.1:n.*7_*8delinsCT
ENST00000326003.6:c.*7_*8delinsCT	ENSP00000314151.1:n.*7_*8delinsCT
ENST00000360617.7:c.1235_1236delinsCT	ENSP00000353829.2:n.1235_1236delinsCT
ENST00000422986.6:c.*449_*450delinsCT	ENSP00000393628.2:n.*449_*450delinsCT
ENST00000595392.5:c.*294_*295delinsCT	ENSP00000468912.1:n.*294_*295delinsCT
ENST00000595952.5:c.*7_*8delinsCT	ENSP00000471155.1:n.*7_*8delinsCT
ENST00000596333.1:n.971_972delinsCT
ENST00000598145.1:c.795_796delinsCT
ENST00000601349.5:n.2072_2073delinsCT
ENST00000617027.4:c.*7_*8delinsCT	ENSP00000483513.1:n.*7_*8delinsCT
NM_001030047.1:c.*518_*519delinsCT	NP_001025218.1:n.*518_*519delinsCT
NM_001030048.1:c.*7_*8delinsCT	NP_001025219.1:n.*7_*8delinsCT
NM_001648.2:c.*7_*8delinsCT MANE Select	NP_001639.1:n.*7_*8delinsCT
XM_011526923.1:c.*7_*8delinsCT	XP_011525225.1:n.*7_*8delinsCT
XR_935817.1:n.1324+880_1324+881delinsCT