Canonical Allele Identifier: CA2586638866
Gene: KLK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50859786A>G , CM000681.2:g.50859786A>G GRCh38
NC_000019.9:g.51363042A>G , CM000681.1:g.51363042A>G GRCh37
NC_000019.8:g.56054854A>G NCBI36
NG_011653.1:g.9872A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.631-186A>G MANE Select ENSP00000314151.1:n.631-186A>G
ENST00000326003.6:c.631-186A>G ENSP00000314151.1:n.631-186A>G
ENST00000360617.7:c.887A>G ENSP00000353829.2:n.887A>G
ENST00000422986.6:c.*287-186A>G ENSP00000393628.2:n.*287-186A>G
ENST00000595392.5:c.*132-186A>G ENSP00000468912.1:n.*132-186A>G
ENST00000595952.5:c.502-186A>G ENSP00000471155.1:n.502-186A>G
ENST00000596185.5:c.*739-186A>G ENSP00000471648.1:n.*739-186A>G
ENST00000596333.1:n.809-186A>G
ENST00000597483.5:c.*170A>G ENSP00000472411.1:n.*170A>G
ENST00000598145.1:c.633-186A>G
ENST00000601349.5:n.1910-186A>G
ENST00000601812.1:n.1063-186A>G
ENST00000617027.4:c.508-186A>G ENSP00000483513.1:n.508-186A>G
NM_001030047.1:c.*170A>G NP_001025218.1:n.*170A>G
NM_001030048.1:c.502-186A>G NP_001025219.1:n.502-186A>G
NM_001648.2:c.631-186A>G MANE Select NP_001639.1:n.631-186A>G
XM_011526923.1:c.649-186A>G XP_011525225.1:n.649-186A>G
XM_011526924.1:c.*170A>G XP_011525226.1:n.*170A>G
XR_935817.1:n.1324+532A>G