Canonical Allele Identifier: CA9604591
Gene: KLK3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2405938
ClinVar RCV Id: RCV004241767
dbSNP Id: rs138882542

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50860021C>T , CM000681.2:g.50860021C>T GRCh38
NC_000019.9:g.51363277C>T , CM000681.1:g.51363277C>T GRCh37
NC_000019.8:g.56055089C>T NCBI36
NG_011653.1:g.10107C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.680C>T MANE Select ENSP00000314151.1:p.Thr227Met
ENST00000326003.6:c.680C>T ENSP00000314151.1:p.Thr227Met
ENST00000360617.7:c.1122C>T ENSP00000353829.2:n.1122C>T
ENST00000422986.6:c.*336C>T ENSP00000393628.2:n.*336C>T
ENST00000595392.5:c.*181C>T ENSP00000468912.1:n.*181C>T
ENST00000595952.5:c.551C>T ENSP00000471155.1:p.Thr184Met
ENST00000596333.1:n.858C>T
ENST00000598145.1:c.682C>T
ENST00000601349.5:n.1959C>T
ENST00000601812.1:n.1112C>T
ENST00000617027.4:c.557C>T ENSP00000483513.1:p.Thr186Met
NM_001030047.1:c.*405C>T NP_001025218.1:n.*405C>T
NM_001030048.1:c.551C>T NP_001025219.1:p.Thr184Met
NM_001648.2:c.680C>T MANE Select NP_001639.1:p.Thr227Met
XM_011526923.1:c.698C>T XP_011525225.1:p.Thr233Met
XR_935817.1:n.1324+767C>T