Canonical Allele Identifier: CA2341114541
Gene: KLK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50858123T= , CM000681.2:g.50858123T= GRCh38
NC_000019.9:g.51361379T= , CM000681.1:g.51361379T= GRCh37
NC_000019.8:g.56053191T= NCBI36
NG_011653.1:g.8209T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.301T= MANE Select ENSP00000314151.1:p.Tyr101=
ENST00000326003.6:c.301T= ENSP00000314151.1:p.Tyr101=
ENST00000360617.7:c.301T= ENSP00000353829.2:p.Tyr101=
ENST00000422986.6:c.265-35T= ENSP00000393628.2:n.265-35T=
ENST00000593997.5:c.301T= ENSP00000472907.1:p.Tyr101=
ENST00000595392.5:c.301T= ENSP00000468912.1:p.Tyr101=
ENST00000595952.5:c.207-35T= ENSP00000471155.1:n.207-35T=
ENST00000596185.5:c.*409T= ENSP00000471648.1:n.*409T=
ENST00000596333.1:n.336T=
ENST00000597286.5:c.190T= ENSP00000470523.1:p.Tyr64=
ENST00000597483.5:c.207-35T= ENSP00000472411.1:n.207-35T=
ENST00000598145.1:c.285T=
ENST00000601349.5:n.1580T=
ENST00000601503.5:c.244T= ENSP00000472213.1:p.Tyr82=
ENST00000601812.1:n.733T=
ENST00000617027.4:c.301T= ENSP00000483513.1:p.Tyr101=
NM_001030047.1:c.301T= NP_001025218.1:p.Tyr101=
NM_001030048.1:c.207-35T= NP_001025219.1:n.207-35T=
NM_001648.2:c.301T= MANE Select NP_001639.1:p.Tyr101=
XM_011526923.1:c.301T= XP_011525225.1:p.Tyr101=
XM_011526924.1:c.301T= XP_011525226.1:p.Tyr101=
XR_935817.1:n.336T=