Canonical Allele Identifier: CA883233078

Gene: KLK2

Linked Data

• dbSNP Id: rs1191355079
• gnomAD v3: 19-50879822-GA-G
• gnomAD v4: 19-50879822-GA-G
• MyVariant Identifiers: chr19:g.51383079del (hg19) ; chr19:g.50879823del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50879824del , CM000681.2:g.50879824del	GRCh38
NC_000019.9:g.51383080del , CM000681.1:g.51383080del	GRCh37
NC_000019.8:g.56074892del	NCBI36
NG_031984.1:g.11392del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325321.8:c.*1265del MANE Select	ENSP00000313581.2:n.*1265del
ENST00000325321.7:c.*1265del	ENSP00000313581.2:n.*1265del
ENST00000358049.8:c.*1416del	ENSP00000350748.3:n.*1416del
ENST00000391810.6:c.*1265del	ENSP00000375686.2:n.*1265del
ENST00000597439.1:c.*1580del	ENSP00000471214.1:n.*1580del
NM_001002231.2:c.*1416del	NP_001002231.1:n.*1416del
NM_001256080.1:c.*1265del	NP_001243009.1:n.*1265del
NM_005551.4:c.*1265del	NP_005542.1:n.*1265del
NR_045762.1:n.2116del
NR_045763.1:n.2178del
NM_005551.5:c.*1265del MANE Select	NP_005542.1:n.*1265del
NM_001002231.3:c.*1416del	NP_001002231.1:n.*1416del
NR_045762.2:n.2110del
NR_045763.2:n.2172del
NM_001256080.2:c.*1265del	NP_001243009.1:n.*1265del