Canonical Allele Identifier: CA2814740537
Gene: KLK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50859749T>A , CM000681.2:g.50859749T>A GRCh38
NC_000019.9:g.51363005T>A , CM000681.1:g.51363005T>A GRCh37
NC_000019.8:g.56054817T>A NCBI36
NG_011653.1:g.9835T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.631-223T>A MANE Select ENSP00000314151.1:n.631-223T>A
ENST00000326003.6:c.631-223T>A ENSP00000314151.1:n.631-223T>A
ENST00000360617.7:c.850T>A ENSP00000353829.2:n.850T>A
ENST00000422986.6:c.*287-223T>A ENSP00000393628.2:n.*287-223T>A
ENST00000595392.5:c.*132-223T>A ENSP00000468912.1:n.*132-223T>A
ENST00000595952.5:c.502-223T>A ENSP00000471155.1:n.502-223T>A
ENST00000596185.5:c.*739-223T>A ENSP00000471648.1:n.*739-223T>A
ENST00000596333.1:n.809-223T>A
ENST00000597483.5:c.*133T>A ENSP00000472411.1:n.*133T>A
ENST00000598145.1:c.633-223T>A
ENST00000601349.5:n.1910-223T>A
ENST00000601812.1:n.1063-223T>A
ENST00000617027.4:c.508-223T>A ENSP00000483513.1:n.508-223T>A
NM_001030047.1:c.*133T>A NP_001025218.1:n.*133T>A
NM_001030048.1:c.502-223T>A NP_001025219.1:n.502-223T>A
NM_001648.2:c.631-223T>A MANE Select NP_001639.1:n.631-223T>A
XM_011526923.1:c.649-223T>A XP_011525225.1:n.649-223T>A
XM_011526924.1:c.*133T>A XP_011525226.1:n.*133T>A
XR_935817.1:n.1324+495T>A