Canonical Allele Identifier: CA2341125198
Gene: KLK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50879728C= , CM000681.2:g.50879728C= GRCh38
NC_000019.9:g.51382984C= , CM000681.1:g.51382984C= GRCh37
NC_000019.8:g.56074796C= NCBI36
NG_031984.1:g.11296C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325321.8:c.*1169C= MANE Select ENSP00000313581.2:n.*1169C=
ENST00000325321.7:c.*1169C= ENSP00000313581.2:n.*1169C=
ENST00000358049.8:c.*1320C= ENSP00000350748.3:n.*1320C=
ENST00000391810.6:c.*1169C= ENSP00000375686.2:n.*1169C=
ENST00000597439.1:c.*1484C= ENSP00000471214.1:n.*1484C=
NM_001002231.2:c.*1320C= NP_001002231.1:n.*1320C=
NM_001256080.1:c.*1169C= NP_001243009.1:n.*1169C=
NM_005551.4:c.*1169C= NP_005542.1:n.*1169C=
NR_045762.1:n.2020C=
NR_045763.1:n.2082C=
NM_005551.5:c.*1169C= MANE Select NP_005542.1:n.*1169C=
NM_001002231.3:c.*1320C= NP_001002231.1:n.*1320C=
NR_045762.2:n.2014C=
NR_045763.2:n.2076C=
NM_001256080.2:c.*1169C= NP_001243009.1:n.*1169C=