Canonical Allele Identifier: CA2341114409
Gene: KLK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50857841C= , CM000681.2:g.50857841C= GRCh38
NC_000019.9:g.51361097C= , CM000681.1:g.51361097C= GRCh37
NC_000019.8:g.56052909C= NCBI36
NG_011653.1:g.7927C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.207-188C= MANE Select ENSP00000314151.1:n.207-188C=
ENST00000326003.6:c.207-188C= ENSP00000314151.1:n.207-188C=
ENST00000360617.7:c.207-188C= ENSP00000353829.2:n.207-188C=
ENST00000422986.6:c.207-188C= ENSP00000393628.2:n.207-188C=
ENST00000593997.5:c.207-188C= ENSP00000472907.1:n.207-188C=
ENST00000595392.5:c.207-188C= ENSP00000468912.1:n.207-188C=
ENST00000595952.5:c.207-317C= ENSP00000471155.1:n.207-317C=
ENST00000596185.5:c.*315-188C= ENSP00000471648.1:n.*315-188C=
ENST00000596333.1:n.242-188C=
ENST00000597286.5:c.96-188C= ENSP00000470523.1:n.96-188C=
ENST00000597483.5:c.207-317C= ENSP00000472411.1:n.207-317C=
ENST00000598145.1:c.191-188C=
ENST00000601349.5:n.1486-188C=
ENST00000601503.5:c.150-188C= ENSP00000472213.1:n.150-188C=
ENST00000601812.1:n.451C=
ENST00000617027.4:c.207-188C= ENSP00000483513.1:n.207-188C=
NM_001030047.1:c.207-188C= NP_001025218.1:n.207-188C=
NM_001030048.1:c.207-317C= NP_001025219.1:n.207-317C=
NM_001648.2:c.207-188C= MANE Select NP_001639.1:n.207-188C=
XM_011526923.1:c.207-188C= XP_011525225.1:n.207-188C=
XM_011526924.1:c.207-188C= XP_011525226.1:n.207-188C=
XR_935817.1:n.242-188C=