Canonical Allele Identifier: CA9604619
Gene: KLK3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1288242
ClinVar RCV Id: RCV001707217
dbSNP Id: rs1058205

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50860142C>T , CM000681.2:g.50860142C>T GRCh38
NC_000019.9:g.51363398C>T , CM000681.1:g.51363398C>T GRCh37
NC_000019.8:g.56055210C>T NCBI36
NG_011653.1:g.10228C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000326003.7:c.*15C>T MANE Select ENSP00000314151.1:n.*15C>T
ENST00000326003.6:c.*15C>T ENSP00000314151.1:n.*15C>T
ENST00000360617.7:c.1243C>T ENSP00000353829.2:n.1243C>T
ENST00000422986.6:c.*457C>T ENSP00000393628.2:n.*457C>T
ENST00000595392.5:c.*302C>T ENSP00000468912.1:n.*302C>T
ENST00000595952.5:c.*15C>T ENSP00000471155.1:n.*15C>T
ENST00000596333.1:n.979C>T
ENST00000598145.1:c.803C>T
ENST00000601349.5:n.2080C>T
ENST00000617027.4:c.*15C>T ENSP00000483513.1:n.*15C>T
NM_001030047.1:c.*526C>T NP_001025218.1:n.*526C>T
NM_001030048.1:c.*15C>T NP_001025219.1:n.*15C>T
NM_001648.2:c.*15C>T MANE Select NP_001639.1:n.*15C>T
XM_011526923.1:c.*15C>T XP_011525225.1:n.*15C>T
XR_935817.1:n.1324+888C>T