Canonical Allele Identifier: CA309651082

Gene: KLK2

Linked Data

• dbSNP Id: rs950283397
• gnomAD v3: 19-50879734-T-G
• gnomAD v4: 19-50879734-T-G
• MyVariant Identifiers: chr19:g.51382990T>G (hg19) ; chr19:g.50879734T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50879734T>G , CM000681.2:g.50879734T>G	GRCh38
NC_000019.9:g.51382990T>G , CM000681.1:g.51382990T>G	GRCh37
NC_000019.8:g.56074802T>G	NCBI36
NG_031984.1:g.11302T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325321.8:c.*1175T>G MANE Select	ENSP00000313581.2:n.*1175T>G
ENST00000325321.7:c.*1175T>G	ENSP00000313581.2:n.*1175T>G
ENST00000358049.8:c.*1326T>G	ENSP00000350748.3:n.*1326T>G
ENST00000391810.6:c.*1175T>G	ENSP00000375686.2:n.*1175T>G
ENST00000597439.1:c.*1490T>G	ENSP00000471214.1:n.*1490T>G
NM_001002231.2:c.*1326T>G	NP_001002231.1:n.*1326T>G
NM_001256080.1:c.*1175T>G	NP_001243009.1:n.*1175T>G
NM_005551.4:c.*1175T>G	NP_005542.1:n.*1175T>G
NR_045762.1:n.2026T>G
NR_045763.1:n.2088T>G
NM_005551.5:c.*1175T>G MANE Select	NP_005542.1:n.*1175T>G
NM_001002231.3:c.*1326T>G	NP_001002231.1:n.*1326T>G
NR_045762.2:n.2020T>G
NR_045763.2:n.2082T>G
NM_001256080.2:c.*1175T>G	NP_001243009.1:n.*1175T>G