Canonical Allele Identifier: CA2341125195
Gene: KLK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50879724A= , CM000681.2:g.50879724A= GRCh38
NC_000019.9:g.51382980A= , CM000681.1:g.51382980A= GRCh37
NC_000019.8:g.56074792A= NCBI36
NG_031984.1:g.11292A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325321.8:c.*1165A= MANE Select ENSP00000313581.2:n.*1165A=
ENST00000325321.7:c.*1165A= ENSP00000313581.2:n.*1165A=
ENST00000358049.8:c.*1316A= ENSP00000350748.3:n.*1316A=
ENST00000391810.6:c.*1165A= ENSP00000375686.2:n.*1165A=
ENST00000597439.1:c.*1480A= ENSP00000471214.1:n.*1480A=
NM_001002231.2:c.*1316A= NP_001002231.1:n.*1316A=
NM_001256080.1:c.*1165A= NP_001243009.1:n.*1165A=
NM_005551.4:c.*1165A= NP_005542.1:n.*1165A=
NR_045762.1:n.2016A=
NR_045763.1:n.2078A=
NM_005551.5:c.*1165A= MANE Select NP_005542.1:n.*1165A=
NM_001002231.3:c.*1316A= NP_001002231.1:n.*1316A=
NR_045762.2:n.2010A=
NR_045763.2:n.2072A=
NM_001256080.2:c.*1165A= NP_001243009.1:n.*1165A=