Canonical Allele Identifier: CA883233004

Gene: KLK2

Linked Data

• dbSNP Id: rs570449470
• gnomAD v3: 19-50879616-G-T
• gnomAD v4: 19-50879616-G-T
• MyVariant Identifiers: chr19:g.51382872G>T (hg19) ; chr19:g.50879616G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50879616G>T , CM000681.2:g.50879616G>T	GRCh38
NC_000019.9:g.51382872G>T , CM000681.1:g.51382872G>T	GRCh37
NC_000019.8:g.56074684G>T	NCBI36
NG_031984.1:g.11184G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325321.8:c.*1057G>T MANE Select	ENSP00000313581.2:n.*1057G>T
ENST00000325321.7:c.*1057G>T	ENSP00000313581.2:n.*1057G>T
ENST00000358049.8:c.*1208G>T	ENSP00000350748.3:n.*1208G>T
ENST00000391810.6:c.*1057G>T	ENSP00000375686.2:n.*1057G>T
ENST00000597439.1:c.*1372G>T	ENSP00000471214.1:n.*1372G>T
NM_001002231.2:c.*1208G>T	NP_001002231.1:n.*1208G>T
NM_001256080.1:c.*1057G>T	NP_001243009.1:n.*1057G>T
NM_005551.4:c.*1057G>T	NP_005542.1:n.*1057G>T
NR_045762.1:n.1908G>T
NR_045763.1:n.1970G>T
NM_005551.5:c.*1057G>T MANE Select	NP_005542.1:n.*1057G>T
NM_001002231.3:c.*1208G>T	NP_001002231.1:n.*1208G>T
NR_045762.2:n.1902G>T
NR_045763.2:n.1964G>T
NM_001256080.2:c.*1057G>T	NP_001243009.1:n.*1057G>T