Canonical Allele Identifier: CA2735929354
Gene: KLK3 HGNC NCBI

Linked Data

dbSNP Id: rs2090173371

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50859828G>A , CM000681.2:g.50859828G>A GRCh38
NC_000019.9:g.51363084G>A , CM000681.1:g.51363084G>A GRCh37
NC_000019.8:g.56054896G>A NCBI36
NG_011653.1:g.9914G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.631-144G>A MANE Select ENSP00000314151.1:n.631-144G>A
ENST00000326003.6:c.631-144G>A ENSP00000314151.1:n.631-144G>A
ENST00000360617.7:c.929G>A ENSP00000353829.2:n.929G>A
ENST00000422986.6:c.*287-144G>A ENSP00000393628.2:n.*287-144G>A
ENST00000595392.5:c.*132-144G>A ENSP00000468912.1:n.*132-144G>A
ENST00000595952.5:c.502-144G>A ENSP00000471155.1:n.502-144G>A
ENST00000596185.5:c.*739-144G>A ENSP00000471648.1:n.*739-144G>A
ENST00000596333.1:n.809-144G>A
ENST00000598145.1:c.633-144G>A
ENST00000601349.5:n.1910-144G>A
ENST00000601812.1:n.1063-144G>A
ENST00000617027.4:c.508-144G>A ENSP00000483513.1:n.508-144G>A
NM_001030047.1:c.*212G>A NP_001025218.1:n.*212G>A
NM_001030048.1:c.502-144G>A NP_001025219.1:n.502-144G>A
NM_001648.2:c.631-144G>A MANE Select NP_001639.1:n.631-144G>A
XM_011526923.1:c.649-144G>A XP_011525225.1:n.649-144G>A
XM_011526924.1:c.*212G>A XP_011525226.1:n.*212G>A
XR_935817.1:n.1324+574G>A