Canonical Allele Identifier: CA2586638943
Gene: KLK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50859885A>T , CM000681.2:g.50859885A>T GRCh38
NC_000019.9:g.51363141A>T , CM000681.1:g.51363141A>T GRCh37
NC_000019.8:g.56054953A>T NCBI36
NG_011653.1:g.9971A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.631-87A>T MANE Select ENSP00000314151.1:n.631-87A>T
ENST00000326003.6:c.631-87A>T ENSP00000314151.1:n.631-87A>T
ENST00000360617.7:c.986A>T ENSP00000353829.2:n.986A>T
ENST00000422986.6:c.*287-87A>T ENSP00000393628.2:n.*287-87A>T
ENST00000595392.5:c.*132-87A>T ENSP00000468912.1:n.*132-87A>T
ENST00000595952.5:c.502-87A>T ENSP00000471155.1:n.502-87A>T
ENST00000596185.5:c.*739-87A>T ENSP00000471648.1:n.*739-87A>T
ENST00000596333.1:n.809-87A>T
ENST00000598145.1:c.633-87A>T
ENST00000601349.5:n.1910-87A>T
ENST00000601812.1:n.1063-87A>T
ENST00000617027.4:c.508-87A>T ENSP00000483513.1:n.508-87A>T
NM_001030047.1:c.*269A>T NP_001025218.1:n.*269A>T
NM_001030048.1:c.502-87A>T NP_001025219.1:n.502-87A>T
NM_001648.2:c.631-87A>T MANE Select NP_001639.1:n.631-87A>T
XM_011526923.1:c.649-87A>T XP_011525225.1:n.649-87A>T
XM_011526924.1:c.*269A>T XP_011525226.1:n.*269A>T
XR_935817.1:n.1324+631A>T