Canonical Allele Identifier: CA2341115652
Gene: KLK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50860216T= , CM000681.2:g.50860216T= GRCh38
NC_000019.9:g.51363472T= , CM000681.1:g.51363472T= GRCh37
NC_000019.8:g.56055284T= NCBI36
NG_011653.1:g.10302T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.*89T= MANE Select ENSP00000314151.1:n.*89T=
ENST00000326003.6:c.*89T= ENSP00000314151.1:n.*89T=
ENST00000360617.7:c.1317T= ENSP00000353829.2:n.1317T=
ENST00000422986.6:c.*531T= ENSP00000393628.2:n.*531T=
ENST00000595392.5:c.*376T= ENSP00000468912.1:n.*376T=
ENST00000595952.5:c.*89T= ENSP00000471155.1:n.*89T=
ENST00000596333.1:n.1053T=
ENST00000601349.5:n.2154T=
ENST00000617027.4:c.*89T= ENSP00000483513.1:n.*89T=
NM_001030047.1:c.*600T= NP_001025218.1:n.*600T=
NM_001030048.1:c.*89T= NP_001025219.1:n.*89T=
NM_001648.2:c.*89T= MANE Select NP_001639.1:n.*89T=
XM_011526923.1:c.*89T= XP_011525225.1:n.*89T=
XR_935817.1:n.1324+962T=