Canonical Allele Identifier: CA407022239
Gene: KLK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50858114C>T , CM000681.2:g.50858114C>T GRCh38
NC_000019.9:g.51361370C>T , CM000681.1:g.51361370C>T GRCh37
NC_000019.8:g.56053182C>T NCBI36
NG_011653.1:g.8200C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.292C>T MANE Select ENSP00000314151.1:p.His98Tyr
ENST00000326003.6:c.292C>T ENSP00000314151.1:p.His98Tyr
ENST00000360617.7:c.292C>T ENSP00000353829.2:p.His98Tyr
ENST00000422986.6:c.264+28C>T ENSP00000393628.2:n.264+28C>T
ENST00000593997.5:c.292C>T ENSP00000472907.1:p.His98Tyr
ENST00000595392.5:c.292C>T ENSP00000468912.1:p.His98Tyr
ENST00000595952.5:c.207-44C>T ENSP00000471155.1:n.207-44C>T
ENST00000596185.5:c.*400C>T ENSP00000471648.1:n.*400C>T
ENST00000596333.1:n.327C>T
ENST00000597286.5:c.181C>T ENSP00000470523.1:p.His61Tyr
ENST00000597483.5:c.207-44C>T ENSP00000472411.1:n.207-44C>T
ENST00000598145.1:c.276C>T
ENST00000601349.5:n.1571C>T
ENST00000601503.5:c.235C>T ENSP00000472213.1:p.His79Tyr
ENST00000601812.1:n.724C>T
ENST00000617027.4:c.292C>T ENSP00000483513.1:p.His98Tyr
NM_001030047.1:c.292C>T NP_001025218.1:p.His98Tyr
NM_001030048.1:c.207-44C>T NP_001025219.1:n.207-44C>T
NM_001648.2:c.292C>T MANE Select NP_001639.1:p.His98Tyr
XM_011526923.1:c.292C>T XP_011525225.1:p.His98Tyr
XM_011526924.1:c.292C>T XP_011525226.1:p.His98Tyr
XR_935817.1:n.327C>T