Canonical Allele Identifier: CA633707236

Gene: KLK2

Linked Data

• dbSNP Id: rs1431572905
• gnomAD v2: 19-51382929-G-A
• gnomAD v3: 19-50879673-G-A
• gnomAD v4: 19-50879673-G-A
• MyVariant Identifiers: chr19:g.51382929G>A (hg19) ; chr19:g.50879673G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50879673G>A , CM000681.2:g.50879673G>A	GRCh38
NC_000019.9:g.51382929G>A , CM000681.1:g.51382929G>A	GRCh37
NC_000019.8:g.56074741G>A	NCBI36
NG_031984.1:g.11241G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325321.8:c.*1114G>A MANE Select	ENSP00000313581.2:n.*1114G>A
ENST00000325321.7:c.*1114G>A	ENSP00000313581.2:n.*1114G>A
ENST00000358049.8:c.*1265G>A	ENSP00000350748.3:n.*1265G>A
ENST00000391810.6:c.*1114G>A	ENSP00000375686.2:n.*1114G>A
ENST00000597439.1:c.*1429G>A	ENSP00000471214.1:n.*1429G>A
NM_001002231.2:c.*1265G>A	NP_001002231.1:n.*1265G>A
NM_001256080.1:c.*1114G>A	NP_001243009.1:n.*1114G>A
NM_005551.4:c.*1114G>A	NP_005542.1:n.*1114G>A
NR_045762.1:n.1965G>A
NR_045763.1:n.2027G>A
NM_005551.5:c.*1114G>A MANE Select	NP_005542.1:n.*1114G>A
NM_001002231.3:c.*1265G>A	NP_001002231.1:n.*1265G>A
NR_045762.2:n.1959G>A
NR_045763.2:n.2021G>A
NM_001256080.2:c.*1114G>A	NP_001243009.1:n.*1114G>A