Canonical Allele Identifier: CA2586645586
Gene: KLK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50879827A>G , CM000681.2:g.50879827A>G GRCh38
NC_000019.9:g.51383083A>G , CM000681.1:g.51383083A>G GRCh37
NC_000019.8:g.56074895A>G NCBI36
NG_031984.1:g.11395A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000325321.8:c.*1268A>G MANE Select ENSP00000313581.2:n.*1268A>G
ENST00000325321.7:c.*1268A>G ENSP00000313581.2:n.*1268A>G
ENST00000358049.8:c.*1419A>G ENSP00000350748.3:n.*1419A>G
ENST00000391810.6:c.*1268A>G ENSP00000375686.2:n.*1268A>G
ENST00000597439.1:c.*1583A>G ENSP00000471214.1:n.*1583A>G
NM_001002231.2:c.*1419A>G NP_001002231.1:n.*1419A>G
NM_001256080.1:c.*1268A>G NP_001243009.1:n.*1268A>G
NM_005551.4:c.*1268A>G NP_005542.1:n.*1268A>G
NR_045762.1:n.2119A>G
NR_045763.1:n.2181A>G
NM_005551.5:c.*1268A>G MANE Select NP_005542.1:n.*1268A>G
NM_001002231.3:c.*1419A>G NP_001002231.1:n.*1419A>G
NR_045762.2:n.2113A>G
NR_045763.2:n.2175A>G
NM_001256080.2:c.*1268A>G NP_001243009.1:n.*1268A>G