Canonical Allele Identifier: CA633707304

Gene: KLK2

Linked Data

• dbSNP Id: rs1424443681
• gnomAD v2: 19-51383116-G-A
• gnomAD v3: 19-50879860-G-A
• gnomAD v4: 19-50879860-G-A
• MyVariant Identifiers: chr19:g.51383116G>A (hg19) ; chr19:g.50879860G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50879860G>A , CM000681.2:g.50879860G>A	GRCh38
NC_000019.9:g.51383116G>A , CM000681.1:g.51383116G>A	GRCh37
NC_000019.8:g.56074928G>A	NCBI36
NG_031984.1:g.11428G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325321.8:c.*1301G>A MANE Select	ENSP00000313581.2:n.*1301G>A
ENST00000325321.7:c.*1301G>A	ENSP00000313581.2:n.*1301G>A
ENST00000358049.8:c.*1452G>A	ENSP00000350748.3:n.*1452G>A
ENST00000391810.6:c.*1301G>A	ENSP00000375686.2:n.*1301G>A
ENST00000597439.1:c.*1616G>A	ENSP00000471214.1:n.*1616G>A
NM_001002231.2:c.*1452G>A	NP_001002231.1:n.*1452G>A
NM_001256080.1:c.*1301G>A	NP_001243009.1:n.*1301G>A
NM_005551.4:c.*1301G>A	NP_005542.1:n.*1301G>A
NR_045762.1:n.2152G>A
NR_045763.1:n.2214G>A
NM_005551.5:c.*1301G>A MANE Select	NP_005542.1:n.*1301G>A
NM_001002231.3:c.*1452G>A	NP_001002231.1:n.*1452G>A
NR_045762.2:n.2146G>A
NR_045763.2:n.2208G>A
NM_001256080.2:c.*1301G>A	NP_001243009.1:n.*1301G>A