Canonical Allele Identifier: CA2341115438
Gene: KLK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50859782C= , CM000681.2:g.50859782C= GRCh38
NC_000019.9:g.51363038C= , CM000681.1:g.51363038C= GRCh37
NC_000019.8:g.56054850C= NCBI36
NG_011653.1:g.9868C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.631-190C= MANE Select ENSP00000314151.1:n.631-190C=
ENST00000326003.6:c.631-190C= ENSP00000314151.1:n.631-190C=
ENST00000360617.7:c.883C= ENSP00000353829.2:n.883C=
ENST00000422986.6:c.*287-190C= ENSP00000393628.2:n.*287-190C=
ENST00000595392.5:c.*132-190C= ENSP00000468912.1:n.*132-190C=
ENST00000595952.5:c.502-190C= ENSP00000471155.1:n.502-190C=
ENST00000596185.5:c.*739-190C= ENSP00000471648.1:n.*739-190C=
ENST00000596333.1:n.809-190C=
ENST00000597483.5:c.*166C= ENSP00000472411.1:n.*166C=
ENST00000598145.1:c.633-190C=
ENST00000601349.5:n.1910-190C=
ENST00000601812.1:n.1063-190C=
ENST00000617027.4:c.508-190C= ENSP00000483513.1:n.508-190C=
NM_001030047.1:c.*166C= NP_001025218.1:n.*166C=
NM_001030048.1:c.502-190C= NP_001025219.1:n.502-190C=
NM_001648.2:c.631-190C= MANE Select NP_001639.1:n.631-190C=
XM_011526923.1:c.649-190C= XP_011525225.1:n.649-190C=
XM_011526924.1:c.*166C= XP_011525226.1:n.*166C=
XR_935817.1:n.1324+528C=