Canonical Allele Identifier: CA2586645599

Gene: KLK2

Linked Data

• gnomAD v4: 19-50879844-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50879844A>G , CM000681.2:g.50879844A>G	GRCh38
NC_000019.9:g.51383100A>G , CM000681.1:g.51383100A>G	GRCh37
NC_000019.8:g.56074912A>G	NCBI36
NG_031984.1:g.11412A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325321.8:c.*1285A>G MANE Select	ENSP00000313581.2:n.*1285A>G
ENST00000325321.7:c.*1285A>G	ENSP00000313581.2:n.*1285A>G
ENST00000358049.8:c.*1436A>G	ENSP00000350748.3:n.*1436A>G
ENST00000391810.6:c.*1285A>G	ENSP00000375686.2:n.*1285A>G
ENST00000597439.1:c.*1600A>G	ENSP00000471214.1:n.*1600A>G
NM_001002231.2:c.*1436A>G	NP_001002231.1:n.*1436A>G
NM_001256080.1:c.*1285A>G	NP_001243009.1:n.*1285A>G
NM_005551.4:c.*1285A>G	NP_005542.1:n.*1285A>G
NR_045762.1:n.2136A>G
NR_045763.1:n.2198A>G
NM_005551.5:c.*1285A>G MANE Select	NP_005542.1:n.*1285A>G
NM_001002231.3:c.*1436A>G	NP_001002231.1:n.*1436A>G
NR_045762.2:n.2130A>G
NR_045763.2:n.2192A>G
NM_001256080.2:c.*1285A>G	NP_001243009.1:n.*1285A>G