Canonical Allele Identifier: CA407024835
Gene: KLK3 HGNC NCBI

Linked Data

dbSNP Id: rs1332251722

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50859979C>A , CM000681.2:g.50859979C>A GRCh38
NC_000019.9:g.51363235C>A , CM000681.1:g.51363235C>A GRCh37
NC_000019.8:g.56055047C>A NCBI36
NG_011653.1:g.10065C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.638C>A MANE Select ENSP00000314151.1:p.Ser213Tyr
ENST00000326003.6:c.638C>A ENSP00000314151.1:p.Ser213Tyr
ENST00000360617.7:c.1080C>A ENSP00000353829.2:n.1080C>A
ENST00000422986.6:c.*294C>A ENSP00000393628.2:n.*294C>A
ENST00000595392.5:c.*139C>A ENSP00000468912.1:n.*139C>A
ENST00000595952.5:c.509C>A ENSP00000471155.1:p.Ser170Tyr
ENST00000596185.5:c.*746C>A ENSP00000471648.1:n.*746C>A
ENST00000596333.1:n.816C>A
ENST00000598145.1:c.640C>A
ENST00000601349.5:n.1917C>A
ENST00000601812.1:n.1070C>A
ENST00000617027.4:c.515C>A ENSP00000483513.1:p.Ser172Tyr
NM_001030047.1:c.*363C>A NP_001025218.1:n.*363C>A
NM_001030048.1:c.509C>A NP_001025219.1:p.Ser170Tyr
NM_001648.2:c.638C>A MANE Select NP_001639.1:p.Ser213Tyr
XM_011526923.1:c.656C>A XP_011525225.1:p.Ser219Tyr
XM_011526924.1:c.*363C>A XP_011525226.1:n.*363C>A
XR_935817.1:n.1324+725C>A