Canonical Allele Identifier: CA2586638980
Gene: KLK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50860228_50860229del , CM000681.2:g.50860228_50860229del GRCh38
NC_000019.9:g.51363484_51363485del , CM000681.1:g.51363484_51363485del GRCh37
NC_000019.8:g.56055296_56055297del NCBI36
NG_011653.1:g.10314_10315del

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.*101_*102del MANE Select ENSP00000314151.1:n.*101_*102del
ENST00000326003.6:c.*101_*102del ENSP00000314151.1:n.*101_*102del
ENST00000360617.7:c.1329_1330del ENSP00000353829.2:n.1329_1330del
ENST00000422986.6:c.*543_*544del ENSP00000393628.2:n.*543_*544del
ENST00000595392.5:c.*388_*389del ENSP00000468912.1:n.*388_*389del
ENST00000595952.5:c.*101_*102del ENSP00000471155.1:n.*101_*102del
ENST00000596333.1:n.1065_1066del
ENST00000601349.5:n.2166_2167del
ENST00000617027.4:c.*101_*102del ENSP00000483513.1:n.*101_*102del
NM_001030047.1:c.*612_*613del NP_001025218.1:n.*612_*613del
NM_001030048.1:c.*101_*102del NP_001025219.1:n.*101_*102del
NM_001648.2:c.*101_*102del MANE Select NP_001639.1:n.*101_*102del
XM_011526923.1:c.*101_*102del XP_011525225.1:n.*101_*102del
XR_935817.1:n.1324+974_1324+975del