Canonical Allele Identifier: CA2814740579
Gene: KLK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50860402_50860403insTTTTAAA , CM000681.2:g.50860402_50860403insTTTTAAA GRCh38
NC_000019.9:g.51363658_51363659insTTTTAAA , CM000681.1:g.51363658_51363659insTTTTAAA GRCh37
NC_000019.8:g.56055470_56055471insTTTTAAA NCBI36
NG_011653.1:g.10488_10489insTTTTAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.*275_*276insTTTTAAA MANE Select ENSP00000314151.1:n.*275_*276insTTTTAAA
ENST00000326003.6:c.*275_*276insTTTTAAA ENSP00000314151.1:n.*275_*276insTTTTAAA
ENST00000360617.7:c.1503_1504insTTTTAAA ENSP00000353829.2:n.1503_1504insTTTTAAA
ENST00000422986.6:c.*717_*718insTTTTAAA ENSP00000393628.2:n.*717_*718insTTTTAAA
ENST00000595952.5:c.*275_*276insTTTTAAA ENSP00000471155.1:n.*275_*276insTTTTAAA
ENST00000596333.1:n.1239_1240insTTTTAAA
ENST00000601349.5:n.2340_2341insTTTTAAA
ENST00000617027.4:c.*275_*276insTTTTAAA ENSP00000483513.1:n.*275_*276insTTTTAAA
NM_001030047.1:c.*786_*787insTTTTAAA NP_001025218.1:n.*786_*787insTTTTAAA
NM_001030048.1:c.*275_*276insTTTTAAA NP_001025219.1:n.*275_*276insTTTTAAA
NM_001648.2:c.*275_*276insTTTTAAA MANE Select NP_001639.1:n.*275_*276insTTTTAAA
XM_011526923.1:c.*275_*276insTTTTAAA XP_011525225.1:n.*275_*276insTTTTAAA
XR_935817.1:n.1324+1148_1324+1149insTTTTAAA