Canonical Allele Identifier: CA2814740538
Gene: KLK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50859752_50859759del , CM000681.2:g.50859752_50859759del GRCh38
NC_000019.9:g.51363008_51363015del , CM000681.1:g.51363008_51363015del GRCh37
NC_000019.8:g.56054820_56054827del NCBI36
NG_011653.1:g.9838_9845del

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.631-220_631-213del MANE Select ENSP00000314151.1:n.631-220_631-213del
ENST00000326003.6:c.631-220_631-213del ENSP00000314151.1:n.631-220_631-213del
ENST00000360617.7:c.853_860del ENSP00000353829.2:n.853_860del
ENST00000422986.6:c.*287-220_*287-213del ENSP00000393628.2:n.*287-220_*287-213del
ENST00000595392.5:c.*132-220_*132-213del ENSP00000468912.1:n.*132-220_*132-213del
ENST00000595952.5:c.502-220_502-213del ENSP00000471155.1:n.502-220_502-213del
ENST00000596185.5:c.*739-220_*739-213del ENSP00000471648.1:n.*739-220_*739-213del
ENST00000596333.1:n.809-220_809-213del
ENST00000597483.5:c.*136_*143del ENSP00000472411.1:n.*136_*143del
ENST00000598145.1:c.633-220_633-213del
ENST00000601349.5:n.1910-220_1910-213del
ENST00000601812.1:n.1063-220_1063-213del
ENST00000617027.4:c.508-220_508-213del ENSP00000483513.1:n.508-220_508-213del
NM_001030047.1:c.*136_*143del NP_001025218.1:n.*136_*143del
NM_001030048.1:c.502-220_502-213del NP_001025219.1:n.502-220_502-213del
NM_001648.2:c.631-220_631-213del MANE Select NP_001639.1:n.631-220_631-213del
XM_011526923.1:c.649-220_649-213del XP_011525225.1:n.649-220_649-213del
XM_011526924.1:c.*136_*143del XP_011525226.1:n.*136_*143del
XR_935817.1:n.1324+498_1324+505del