Canonical Allele Identifier: CA657458979
Gene: KLK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50860210_50860211insT , CM000681.2:g.50860210_50860211insT GRCh38
NC_000019.9:g.51363466_51363467insT , CM000681.1:g.51363466_51363467insT GRCh37
NC_000019.8:g.56055278_56055279insT NCBI36
NG_011653.1:g.10296_10297insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.*83_*84insT MANE Select ENSP00000314151.1:n.*83_*84insT
ENST00000326003.6:c.*83_*84insT ENSP00000314151.1:n.*83_*84insT
ENST00000360617.7:c.1311_1312insT ENSP00000353829.2:n.1311_1312insT
ENST00000422986.6:c.*525_*526insT ENSP00000393628.2:n.*525_*526insT
ENST00000595392.5:c.*370_*371insT ENSP00000468912.1:n.*370_*371insT
ENST00000595952.5:c.*83_*84insT ENSP00000471155.1:n.*83_*84insT
ENST00000596333.1:n.1047_1048insT
ENST00000601349.5:n.2148_2149insT
ENST00000617027.4:c.*83_*84insT ENSP00000483513.1:n.*83_*84insT
NM_001030047.1:c.*594_*595insT NP_001025218.1:n.*594_*595insT
NM_001030048.1:c.*83_*84insT NP_001025219.1:n.*83_*84insT
NM_001648.2:c.*83_*84insT MANE Select NP_001639.1:n.*83_*84insT
XM_011526923.1:c.*83_*84insT XP_011525225.1:n.*83_*84insT
XR_935817.1:n.1324+956_1324+957insT