Canonical Allele Identifier: CA2586638794

Gene: KLK3

Linked Data

• gnomAD v4: 19-50859730-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50859731del , CM000681.2:g.50859731del	GRCh38
NC_000019.9:g.51362987del , CM000681.1:g.51362987del	GRCh37
NC_000019.8:g.56054799del	NCBI36
NG_011653.1:g.9817del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.631-241del MANE Select	ENSP00000314151.1:n.631-241del
ENST00000326003.6:c.631-241del	ENSP00000314151.1:n.631-241del
ENST00000360617.7:c.832del	ENSP00000353829.2:n.832del
ENST00000422986.6:c.*287-241del	ENSP00000393628.2:n.*287-241del
ENST00000595392.5:c.*132-241del	ENSP00000468912.1:n.*132-241del
ENST00000595952.5:c.502-241del	ENSP00000471155.1:n.502-241del
ENST00000596185.5:c.*739-241del	ENSP00000471648.1:n.*739-241del
ENST00000596333.1:n.809-241del
ENST00000597483.5:c.*115del	ENSP00000472411.1:n.*115del
ENST00000598145.1:c.633-241del
ENST00000601349.5:n.1910-241del
ENST00000601812.1:n.1063-241del
ENST00000617027.4:c.508-241del	ENSP00000483513.1:n.508-241del
NM_001030047.1:c.*115del	NP_001025218.1:n.*115del
NM_001030048.1:c.502-241del	NP_001025219.1:n.502-241del
NM_001648.2:c.631-241del MANE Select	NP_001639.1:n.631-241del
XM_011526923.1:c.649-241del	XP_011525225.1:n.649-241del
XM_011526924.1:c.*115del	XP_011525226.1:n.*115del
XR_935817.1:n.1324+477del