Canonical Allele Identifier: CA2341114537
Gene: KLK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50858117C= , CM000681.2:g.50858117C= GRCh38
NC_000019.9:g.51361373C= , CM000681.1:g.51361373C= GRCh37
NC_000019.8:g.56053185C= NCBI36
NG_011653.1:g.8203C=

Transcript Alleles

HGVS Amino-acid change
ENST00000326003.7:c.295C= MANE Select ENSP00000314151.1:p.Pro99=
ENST00000326003.6:c.295C= ENSP00000314151.1:p.Pro99=
ENST00000360617.7:c.295C= ENSP00000353829.2:p.Pro99=
ENST00000422986.6:c.264+31C= ENSP00000393628.2:n.264+31C=
ENST00000593997.5:c.295C= ENSP00000472907.1:p.Pro99=
ENST00000595392.5:c.295C= ENSP00000468912.1:p.Pro99=
ENST00000595952.5:c.207-41C= ENSP00000471155.1:n.207-41C=
ENST00000596185.5:c.*403C= ENSP00000471648.1:n.*403C=
ENST00000596333.1:n.330C=
ENST00000597286.5:c.184C= ENSP00000470523.1:p.Pro62=
ENST00000597483.5:c.207-41C= ENSP00000472411.1:n.207-41C=
ENST00000598145.1:c.279C=
ENST00000601349.5:n.1574C=
ENST00000601503.5:c.238C= ENSP00000472213.1:p.Pro80=
ENST00000601812.1:n.727C=
ENST00000617027.4:c.295C= ENSP00000483513.1:p.Pro99=
NM_001030047.1:c.295C= NP_001025218.1:p.Pro99=
NM_001030048.1:c.207-41C= NP_001025219.1:n.207-41C=
NM_001648.2:c.295C= MANE Select NP_001639.1:p.Pro99=
XM_011526923.1:c.295C= XP_011525225.1:p.Pro99=
XM_011526924.1:c.295C= XP_011525226.1:p.Pro99=
XR_935817.1:n.330C=