Canonical Allele Identifier: CA2586645522

Gene: KLK2

Linked Data

• gnomAD v4: 19-50879661-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50879661C>A , CM000681.2:g.50879661C>A	GRCh38
NC_000019.9:g.51382917C>A , CM000681.1:g.51382917C>A	GRCh37
NC_000019.8:g.56074729C>A	NCBI36
NG_031984.1:g.11229C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325321.8:c.*1102C>A MANE Select	ENSP00000313581.2:n.*1102C>A
ENST00000325321.7:c.*1102C>A	ENSP00000313581.2:n.*1102C>A
ENST00000358049.8:c.*1253C>A	ENSP00000350748.3:n.*1253C>A
ENST00000391810.6:c.*1102C>A	ENSP00000375686.2:n.*1102C>A
ENST00000597439.1:c.*1417C>A	ENSP00000471214.1:n.*1417C>A
NM_001002231.2:c.*1253C>A	NP_001002231.1:n.*1253C>A
NM_001256080.1:c.*1102C>A	NP_001243009.1:n.*1102C>A
NM_005551.4:c.*1102C>A	NP_005542.1:n.*1102C>A
NR_045762.1:n.1953C>A
NR_045763.1:n.2015C>A
NM_005551.5:c.*1102C>A MANE Select	NP_005542.1:n.*1102C>A
NM_001002231.3:c.*1253C>A	NP_001002231.1:n.*1253C>A
NR_045762.2:n.1947C>A
NR_045763.2:n.2009C>A
NM_001256080.2:c.*1102C>A	NP_001243009.1:n.*1102C>A