Canonical Allele Identifier: CA2341125158

Gene: KLK2

Linked Data

• dbSNP Id: rs2090322901

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50879656A>C , CM000681.2:g.50879656A>C	GRCh38
NC_000019.9:g.51382912A>C , CM000681.1:g.51382912A>C	GRCh37
NC_000019.8:g.56074724A>C	NCBI36
NG_031984.1:g.11224A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325321.8:c.*1097A>C MANE Select	ENSP00000313581.2:n.*1097A>C
ENST00000325321.7:c.*1097A>C	ENSP00000313581.2:n.*1097A>C
ENST00000358049.8:c.*1248A>C	ENSP00000350748.3:n.*1248A>C
ENST00000391810.6:c.*1097A>C	ENSP00000375686.2:n.*1097A>C
ENST00000597439.1:c.*1412A>C	ENSP00000471214.1:n.*1412A>C
NM_001002231.2:c.*1248A>C	NP_001002231.1:n.*1248A>C
NM_001256080.1:c.*1097A>C	NP_001243009.1:n.*1097A>C
NM_005551.4:c.*1097A>C	NP_005542.1:n.*1097A>C
NR_045762.1:n.1948A>C
NR_045763.1:n.2010A>C
NM_005551.5:c.*1097A>C MANE Select	NP_005542.1:n.*1097A>C
NM_001002231.3:c.*1248A>C	NP_001002231.1:n.*1248A>C
NR_045762.2:n.1942A>C
NR_045763.2:n.2004A>C
NM_001256080.2:c.*1097A>C	NP_001243009.1:n.*1097A>C