Canonical Allele Identifier: CA407022237
Gene: KLK3 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.292C>A MANE Select ENSP00000314151.1:p.His98Asn
ENST00000326003.6:c.292C>A ENSP00000314151.1:p.His98Asn
ENST00000360617.7:c.292C>A ENSP00000353829.2:p.His98Asn
ENST00000422986.6:c.264+28C>A ENSP00000393628.2:n.264+28C>A
ENST00000593997.5:c.292C>A ENSP00000472907.1:p.His98Asn
ENST00000595392.5:c.292C>A ENSP00000468912.1:p.His98Asn
ENST00000595952.5:c.207-44C>A ENSP00000471155.1:n.207-44C>A
ENST00000596185.5:c.*400C>A ENSP00000471648.1:n.*400C>A
ENST00000596333.1:n.327C>A
ENST00000597286.5:c.181C>A ENSP00000470523.1:p.His61Asn
ENST00000597483.5:c.207-44C>A ENSP00000472411.1:n.207-44C>A
ENST00000598145.1:c.276C>A
ENST00000601349.5:n.1571C>A
ENST00000601503.5:c.235C>A ENSP00000472213.1:p.His79Asn
ENST00000601812.1:n.724C>A
ENST00000617027.4:c.292C>A ENSP00000483513.1:p.His98Asn
NM_001030047.1:c.292C>A NP_001025218.1:p.His98Asn
NM_001030048.1:c.207-44C>A NP_001025219.1:n.207-44C>A
NM_001648.2:c.292C>A MANE Select NP_001639.1:p.His98Asn
XM_011526923.1:c.292C>A XP_011525225.1:p.His98Asn
XM_011526924.1:c.292C>A XP_011525226.1:p.His98Asn
XR_935817.1:n.327C>A