Canonical Allele Identifier: CA2586638843

Gene: KLK3

Linked Data

• gnomAD v4: 19-50859766-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50859770del , CM000681.2:g.50859770del	GRCh38
NC_000019.9:g.51363026del , CM000681.1:g.51363026del	GRCh37
NC_000019.8:g.56054838del	NCBI36
NG_011653.1:g.9856del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.631-202del MANE Select	ENSP00000314151.1:n.631-202del
ENST00000326003.6:c.631-202del	ENSP00000314151.1:n.631-202del
ENST00000360617.7:c.871del	ENSP00000353829.2:n.871del
ENST00000422986.6:c.*287-202del	ENSP00000393628.2:n.*287-202del
ENST00000595392.5:c.*132-202del	ENSP00000468912.1:n.*132-202del
ENST00000595952.5:c.502-202del	ENSP00000471155.1:n.502-202del
ENST00000596185.5:c.*739-202del	ENSP00000471648.1:n.*739-202del
ENST00000596333.1:n.809-202del
ENST00000597483.5:c.*154del	ENSP00000472411.1:n.*154del
ENST00000598145.1:c.633-202del
ENST00000601349.5:n.1910-202del
ENST00000601812.1:n.1063-202del
ENST00000617027.4:c.508-202del	ENSP00000483513.1:n.508-202del
NM_001030047.1:c.*154del	NP_001025218.1:n.*154del
NM_001030048.1:c.502-202del	NP_001025219.1:n.502-202del
NM_001648.2:c.631-202del MANE Select	NP_001639.1:n.631-202del
XM_011526923.1:c.649-202del	XP_011525225.1:n.649-202del
XM_011526924.1:c.*154del	XP_011525226.1:n.*154del
XR_935817.1:n.1324+516del