Canonical Allele Identifier: CA2341115594
Gene: KLK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50860122C= , CM000681.2:g.50860122C= GRCh38
NC_000019.9:g.51363378C= , CM000681.1:g.51363378C= GRCh37
NC_000019.8:g.56055190C= NCBI36
NG_011653.1:g.10208C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.781C= MANE Select ENSP00000314151.1:p.Pro261=
ENST00000326003.6:c.781C= ENSP00000314151.1:p.Pro261=
ENST00000360617.7:c.1223C= ENSP00000353829.2:n.1223C=
ENST00000422986.6:c.*437C= ENSP00000393628.2:n.*437C=
ENST00000595392.5:c.*282C= ENSP00000468912.1:n.*282C=
ENST00000595952.5:c.652C= ENSP00000471155.1:p.Pro218=
ENST00000596333.1:n.959C=
ENST00000598145.1:c.783C=
ENST00000601349.5:n.2060C=
ENST00000601812.1:n.1213C=
ENST00000617027.4:c.658C= ENSP00000483513.1:p.Pro220=
NM_001030047.1:c.*506C= NP_001025218.1:n.*506C=
NM_001030048.1:c.652C= NP_001025219.1:p.Pro218=
NM_001648.2:c.781C= MANE Select NP_001639.1:p.Pro261=
XM_011526923.1:c.799C= XP_011525225.1:p.Pro267=
XR_935817.1:n.1324+868C=