Canonical Allele Identifier: CA2341115592
Gene: KLK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50860117C= , CM000681.2:g.50860117C= GRCh38
NC_000019.9:g.51363373C= , CM000681.1:g.51363373C= GRCh37
NC_000019.8:g.56055185C= NCBI36
NG_011653.1:g.10203C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.776C= MANE Select ENSP00000314151.1:p.Ala259=
ENST00000326003.6:c.776C= ENSP00000314151.1:p.Ala259=
ENST00000360617.7:c.1218C= ENSP00000353829.2:n.1218C=
ENST00000422986.6:c.*432C= ENSP00000393628.2:n.*432C=
ENST00000595392.5:c.*277C= ENSP00000468912.1:n.*277C=
ENST00000595952.5:c.647C= ENSP00000471155.1:p.Ala216=
ENST00000596333.1:n.954C=
ENST00000598145.1:c.778C=
ENST00000601349.5:n.2055C=
ENST00000601812.1:n.1208C=
ENST00000617027.4:c.653C= ENSP00000483513.1:p.Ala218=
NM_001030047.1:c.*501C= NP_001025218.1:n.*501C=
NM_001030048.1:c.647C= NP_001025219.1:p.Ala216=
NM_001648.2:c.776C= MANE Select NP_001639.1:p.Ala259=
XM_011526923.1:c.794C= XP_011525225.1:p.Ala265=
XR_935817.1:n.1324+863C=