Canonical Allele Identifier: CA883221696
Gene: KLK3 HGNC NCBI

Linked Data

dbSNP Id: rs1424149538

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50859770_50859773del , CM000681.2:g.50859770_50859773del GRCh38
NC_000019.9:g.51363026_51363029del , CM000681.1:g.51363026_51363029del GRCh37
NC_000019.8:g.56054838_56054841del NCBI36
NG_011653.1:g.9856_9859del

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.631-202_631-199del MANE Select ENSP00000314151.1:n.631-202_631-199del
ENST00000326003.6:c.631-202_631-199del ENSP00000314151.1:n.631-202_631-199del
ENST00000360617.7:c.871_874del ENSP00000353829.2:n.871_874del
ENST00000422986.6:c.*287-202_*287-199del ENSP00000393628.2:n.*287-202_*287-199del
ENST00000595392.5:c.*132-202_*132-199del ENSP00000468912.1:n.*132-202_*132-199del
ENST00000595952.5:c.502-202_502-199del ENSP00000471155.1:n.502-202_502-199del
ENST00000596185.5:c.*739-202_*739-199del ENSP00000471648.1:n.*739-202_*739-199del
ENST00000596333.1:n.809-202_809-199del
ENST00000597483.5:c.*154_*157del ENSP00000472411.1:n.*154_*157del
ENST00000598145.1:c.633-202_633-199del
ENST00000601349.5:n.1910-202_1910-199del
ENST00000601812.1:n.1063-202_1063-199del
ENST00000617027.4:c.508-202_508-199del ENSP00000483513.1:n.508-202_508-199del
NM_001030047.1:c.*154_*157del NP_001025218.1:n.*154_*157del
NM_001030048.1:c.502-202_502-199del NP_001025219.1:n.502-202_502-199del
NM_001648.2:c.631-202_631-199del MANE Select NP_001639.1:n.631-202_631-199del
XM_011526923.1:c.649-202_649-199del XP_011525225.1:n.649-202_649-199del
XM_011526924.1:c.*154_*157del XP_011525226.1:n.*154_*157del
XR_935817.1:n.1324+516_1324+519del