Canonical Allele Identifier: CA2341115635
Gene: KLK3 HGNC NCBI

Linked Data

dbSNP Id: rs141498977

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50860186G>A , CM000681.2:g.50860186G>A GRCh38
NC_000019.9:g.51363442G>A , CM000681.1:g.51363442G>A GRCh37
NC_000019.8:g.56055254G>A NCBI36
NG_011653.1:g.10272G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.*59G>A MANE Select ENSP00000314151.1:n.*59G>A
ENST00000326003.6:c.*59G>A ENSP00000314151.1:n.*59G>A
ENST00000360617.7:c.1287G>A ENSP00000353829.2:n.1287G>A
ENST00000422986.6:c.*501G>A ENSP00000393628.2:n.*501G>A
ENST00000595392.5:c.*346G>A ENSP00000468912.1:n.*346G>A
ENST00000595952.5:c.*59G>A ENSP00000471155.1:n.*59G>A
ENST00000596333.1:n.1023G>A
ENST00000598145.1:c.847G>A
ENST00000601349.5:n.2124G>A
ENST00000617027.4:c.*59G>A ENSP00000483513.1:n.*59G>A
NM_001030047.1:c.*570G>A NP_001025218.1:n.*570G>A
NM_001030048.1:c.*59G>A NP_001025219.1:n.*59G>A
NM_001648.2:c.*59G>A MANE Select NP_001639.1:n.*59G>A
XM_011526923.1:c.*59G>A XP_011525225.1:n.*59G>A
XR_935817.1:n.1324+932G>A