Canonical Allele Identifier: CA2341125262
Gene: KLK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50879847T= , CM000681.2:g.50879847T= GRCh38
NC_000019.9:g.51383103T= , CM000681.1:g.51383103T= GRCh37
NC_000019.8:g.56074915T= NCBI36
NG_031984.1:g.11415T=

Transcript Alleles

HGVS Amino-acid change
ENST00000325321.8:c.*1288T= MANE Select ENSP00000313581.2:n.*1288T=
ENST00000325321.7:c.*1288T= ENSP00000313581.2:n.*1288T=
ENST00000358049.8:c.*1439T= ENSP00000350748.3:n.*1439T=
ENST00000391810.6:c.*1288T= ENSP00000375686.2:n.*1288T=
ENST00000597439.1:c.*1603T= ENSP00000471214.1:n.*1603T=
NM_001002231.2:c.*1439T= NP_001002231.1:n.*1439T=
NM_001256080.1:c.*1288T= NP_001243009.1:n.*1288T=
NM_005551.4:c.*1288T= NP_005542.1:n.*1288T=
NR_045762.1:n.2139T=
NR_045763.1:n.2201T=
NM_005551.5:c.*1288T= MANE Select NP_005542.1:n.*1288T=
NM_001002231.3:c.*1439T= NP_001002231.1:n.*1439T=
NR_045762.2:n.2133T=
NR_045763.2:n.2195T=
NM_001256080.2:c.*1288T= NP_001243009.1:n.*1288T=