Canonical Allele Identifier: CA2341114570
Gene: KLK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50858175G= , CM000681.2:g.50858175G= GRCh38
NC_000019.9:g.51361431G= , CM000681.1:g.51361431G= GRCh37
NC_000019.8:g.56053243G= NCBI36
NG_011653.1:g.8261G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.353G= MANE Select ENSP00000314151.1:p.Ser118=
ENST00000326003.6:c.353G= ENSP00000314151.1:p.Ser118=
ENST00000360617.7:c.353G= ENSP00000353829.2:p.Ser118=
ENST00000422986.6:c.*9G= ENSP00000393628.2:n.*9G=
ENST00000593997.5:c.353G= ENSP00000472907.1:p.Ser118=
ENST00000595392.5:c.352+1G= ENSP00000468912.1:n.352+1G=
ENST00000595952.5:c.224G= ENSP00000471155.1:p.Ser75=
ENST00000596185.5:c.*461G= ENSP00000471648.1:n.*461G=
ENST00000596333.1:n.388G=
ENST00000597286.5:c.242G= ENSP00000470523.1:p.Ser81=
ENST00000597483.5:c.224G= ENSP00000472411.1:p.Ser75=
ENST00000598145.1:c.337G=
ENST00000601349.5:n.1632G=
ENST00000601503.5:c.296G= ENSP00000472213.1:p.Ser99=
ENST00000601812.1:n.785G=
ENST00000617027.4:c.353G= ENSP00000483513.1:p.Ser118=
NM_001030047.1:c.353G= NP_001025218.1:p.Ser118=
NM_001030048.1:c.224G= NP_001025219.1:p.Ser75=
NM_001648.2:c.353G= MANE Select NP_001639.1:p.Ser118=
XM_011526923.1:c.353G= XP_011525225.1:p.Ser118=
XM_011526924.1:c.353G= XP_011525226.1:p.Ser118=
XR_935817.1:n.388G=