Canonical Allele Identifier: CA2814740529
Gene: KLK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50859727_50859733del , CM000681.2:g.50859727_50859733del GRCh38
NC_000019.9:g.51362983_51362989del , CM000681.1:g.51362983_51362989del GRCh37
NC_000019.8:g.56054795_56054801del NCBI36
NG_011653.1:g.9813_9819del

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.631-245_631-239del MANE Select ENSP00000314151.1:n.631-245_631-239del
ENST00000326003.6:c.631-245_631-239del ENSP00000314151.1:n.631-245_631-239del
ENST00000360617.7:c.828_834del ENSP00000353829.2:n.828_834del
ENST00000422986.6:c.*287-245_*287-239del ENSP00000393628.2:n.*287-245_*287-239del
ENST00000595392.5:c.*132-245_*132-239del ENSP00000468912.1:n.*132-245_*132-239del
ENST00000595952.5:c.502-245_502-239del ENSP00000471155.1:n.502-245_502-239del
ENST00000596185.5:c.*739-245_*739-239del ENSP00000471648.1:n.*739-245_*739-239del
ENST00000596333.1:n.809-245_809-239del
ENST00000597483.5:c.*111_*117del ENSP00000472411.1:n.*111_*117del
ENST00000598145.1:c.633-245_633-239del
ENST00000601349.5:n.1910-245_1910-239del
ENST00000601812.1:n.1063-245_1063-239del
ENST00000617027.4:c.508-245_508-239del ENSP00000483513.1:n.508-245_508-239del
NM_001030047.1:c.*111_*117del NP_001025218.1:n.*111_*117del
NM_001030048.1:c.502-245_502-239del NP_001025219.1:n.502-245_502-239del
NM_001648.2:c.631-245_631-239del MANE Select NP_001639.1:n.631-245_631-239del
XM_011526923.1:c.649-245_649-239del XP_011525225.1:n.649-245_649-239del
XM_011526924.1:c.*111_*117del XP_011525226.1:n.*111_*117del
XR_935817.1:n.1324+473_1324+479del