Canonical Allele Identifier: CA2341125199
Gene: KLK2 HGNC NCBI

Linked Data

dbSNP Id: rs2090323875

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50879729_50879730del , CM000681.2:g.50879729_50879730del GRCh38
NC_000019.9:g.51382985_51382986del , CM000681.1:g.51382985_51382986del GRCh37
NC_000019.8:g.56074797_56074798del NCBI36
NG_031984.1:g.11297_11298del

Transcript Alleles

HGVS Amino-acid Change
ENST00000325321.8:c.*1170_*1171del MANE Select ENSP00000313581.2:n.*1170_*1171del
ENST00000325321.7:c.*1170_*1171del ENSP00000313581.2:n.*1170_*1171del
ENST00000358049.8:c.*1321_*1322del ENSP00000350748.3:n.*1321_*1322del
ENST00000391810.6:c.*1170_*1171del ENSP00000375686.2:n.*1170_*1171del
ENST00000597439.1:c.*1485_*1486del ENSP00000471214.1:n.*1485_*1486del
NM_001002231.2:c.*1321_*1322del NP_001002231.1:n.*1321_*1322del
NM_001256080.1:c.*1170_*1171del NP_001243009.1:n.*1170_*1171del
NM_005551.4:c.*1170_*1171del NP_005542.1:n.*1170_*1171del
NR_045762.1:n.2021_2022del
NR_045763.1:n.2083_2084del
NM_005551.5:c.*1170_*1171del MANE Select NP_005542.1:n.*1170_*1171del
NM_001002231.3:c.*1321_*1322del NP_001002231.1:n.*1321_*1322del
NR_045762.2:n.2015_2016del
NR_045763.2:n.2077_2078del
NM_001256080.2:c.*1170_*1171del NP_001243009.1:n.*1170_*1171del