Canonical Allele Identifier: CA2341115590

Gene: KLK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860114_50860115delinsTG , CM000681.2:g.50860114_50860115delinsTG	GRCh38
NC_000019.9:g.51363370_51363371delinsTG , CM000681.1:g.51363370_51363371delinsTG	GRCh37
NC_000019.8:g.56055182_56055183delinsTG	NCBI36
NG_011653.1:g.10200_10201delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.773_774delinsTG MANE Select	ENSP00000314151.1:p.Val258=
ENST00000326003.6:c.773_774delinsTG	ENSP00000314151.1:p.Val258=
ENST00000360617.7:c.1215_1216delinsTG	ENSP00000353829.2:n.1215_1216delinsTG
ENST00000422986.6:c.*429_*430delinsTG	ENSP00000393628.2:n.*429_*430delinsTG
ENST00000595392.5:c.*274_*275delinsTG	ENSP00000468912.1:n.*274_*275delinsTG
ENST00000595952.5:c.644_645delinsTG	ENSP00000471155.1:p.Val215=
ENST00000596333.1:n.951_952delinsTG
ENST00000598145.1:c.775_776delinsTG
ENST00000601349.5:n.2052_2053delinsTG
ENST00000601812.1:n.1205_1206delinsTG
ENST00000617027.4:c.650_651delinsTG	ENSP00000483513.1:p.Val217=
NM_001030047.1:c.*498_*499delinsTG	NP_001025218.1:n.*498_*499delinsTG
NM_001030048.1:c.644_645delinsTG	NP_001025219.1:p.Val215=
NM_001648.2:c.773_774delinsTG MANE Select	NP_001639.1:p.Val258=
XM_011526923.1:c.791_792delinsTG	XP_011525225.1:p.Val264=
XR_935817.1:n.1324+860_1324+861delinsTG