Canonical Allele Identifier: CA2341125204
Gene: KLK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50879734T= , CM000681.2:g.50879734T= GRCh38
NC_000019.9:g.51382990T= , CM000681.1:g.51382990T= GRCh37
NC_000019.8:g.56074802T= NCBI36
NG_031984.1:g.11302T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325321.8:c.*1175T= MANE Select ENSP00000313581.2:n.*1175T=
ENST00000325321.7:c.*1175T= ENSP00000313581.2:n.*1175T=
ENST00000358049.8:c.*1326T= ENSP00000350748.3:n.*1326T=
ENST00000391810.6:c.*1175T= ENSP00000375686.2:n.*1175T=
ENST00000597439.1:c.*1490T= ENSP00000471214.1:n.*1490T=
NM_001002231.2:c.*1326T= NP_001002231.1:n.*1326T=
NM_001256080.1:c.*1175T= NP_001243009.1:n.*1175T=
NM_005551.4:c.*1175T= NP_005542.1:n.*1175T=
NR_045762.1:n.2026T=
NR_045763.1:n.2088T=
NM_005551.5:c.*1175T= MANE Select NP_005542.1:n.*1175T=
NM_001002231.3:c.*1326T= NP_001002231.1:n.*1326T=
NR_045762.2:n.2020T=
NR_045763.2:n.2082T=
NM_001256080.2:c.*1175T= NP_001243009.1:n.*1175T=