Canonical Allele Identifier: CA2341125260

Gene: KLK2

Linked Data

• dbSNP Id: rs2090325297

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50879842G>C , CM000681.2:g.50879842G>C	GRCh38
NC_000019.9:g.51383098G>C , CM000681.1:g.51383098G>C	GRCh37
NC_000019.8:g.56074910G>C	NCBI36
NG_031984.1:g.11410G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000325321.8:c.*1283G>C MANE Select	ENSP00000313581.2:n.*1283G>C
ENST00000325321.7:c.*1283G>C	ENSP00000313581.2:n.*1283G>C
ENST00000358049.8:c.*1434G>C	ENSP00000350748.3:n.*1434G>C
ENST00000391810.6:c.*1283G>C	ENSP00000375686.2:n.*1283G>C
ENST00000597439.1:c.*1598G>C	ENSP00000471214.1:n.*1598G>C
NM_001002231.2:c.*1434G>C	NP_001002231.1:n.*1434G>C
NM_001256080.1:c.*1283G>C	NP_001243009.1:n.*1283G>C
NM_005551.4:c.*1283G>C	NP_005542.1:n.*1283G>C
NR_045762.1:n.2134G>C
NR_045763.1:n.2196G>C
NM_005551.5:c.*1283G>C MANE Select	NP_005542.1:n.*1283G>C
NM_001002231.3:c.*1434G>C	NP_001002231.1:n.*1434G>C
NR_045762.2:n.2128G>C
NR_045763.2:n.2190G>C
NM_001256080.2:c.*1283G>C	NP_001243009.1:n.*1283G>C