Canonical Allele Identifier: CA2341114625
Gene: KLK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50858296C= , CM000681.2:g.50858296C= GRCh38
NC_000019.9:g.51361552C= , CM000681.1:g.51361552C= GRCh37
NC_000019.8:g.56053364C= NCBI36
NG_011653.1:g.8382C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.474C= MANE Select ENSP00000314151.1:p.Gly158=
ENST00000326003.6:c.474C= ENSP00000314151.1:p.Gly158=
ENST00000360617.7:c.474C= ENSP00000353829.2:p.Gly158=
ENST00000422986.6:c.*130C= ENSP00000393628.2:n.*130C=
ENST00000593997.5:c.474C= ENSP00000472907.1:p.Gly158=
ENST00000595392.5:c.353-3C= ENSP00000468912.1:n.353-3C=
ENST00000595952.5:c.345C= ENSP00000471155.1:p.Gly115=
ENST00000596185.5:c.*582C= ENSP00000471648.1:n.*582C=
ENST00000596333.1:n.509C=
ENST00000597286.5:c.363C= ENSP00000470523.1:p.Gly121=
ENST00000597483.5:c.345C= ENSP00000472411.1:p.Gly115=
ENST00000598145.1:c.458C=
ENST00000601349.5:n.1753C=
ENST00000601503.5:c.417C= ENSP00000472213.1:p.Gly139=
ENST00000601812.1:n.906C=
ENST00000617027.4:c.354-3C= ENSP00000483513.1:n.354-3C=
NM_001030047.1:c.474C= NP_001025218.1:p.Gly158=
NM_001030048.1:c.345C= NP_001025219.1:p.Gly115=
NM_001648.2:c.474C= MANE Select NP_001639.1:p.Gly158=
XM_011526923.1:c.474C= XP_011525225.1:p.Gly158=
XM_011526924.1:c.474C= XP_011525226.1:p.Gly158=
XR_935817.1:n.509C=