Canonical Allele Identifier: CA883233081

Gene: KLK2

Linked Data

• dbSNP Id: rs1483367296
• MyVariant Identifiers: chr19:g.51383094C>T (hg19) ; chr19:g.50879838C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50879838C>T , CM000681.2:g.50879838C>T	GRCh38
NC_000019.9:g.51383094C>T , CM000681.1:g.51383094C>T	GRCh37
NC_000019.8:g.56074906C>T	NCBI36
NG_031984.1:g.11406C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325321.8:c.*1279C>T MANE Select	ENSP00000313581.2:n.*1279C>T
ENST00000325321.7:c.*1279C>T	ENSP00000313581.2:n.*1279C>T
ENST00000358049.8:c.*1430C>T	ENSP00000350748.3:n.*1430C>T
ENST00000391810.6:c.*1279C>T	ENSP00000375686.2:n.*1279C>T
ENST00000597439.1:c.*1594C>T	ENSP00000471214.1:n.*1594C>T
NM_001002231.2:c.*1430C>T	NP_001002231.1:n.*1430C>T
NM_001256080.1:c.*1279C>T	NP_001243009.1:n.*1279C>T
NM_005551.4:c.*1279C>T	NP_005542.1:n.*1279C>T
NR_045762.1:n.2130C>T
NR_045763.1:n.2192C>T
NM_005551.5:c.*1279C>T MANE Select	NP_005542.1:n.*1279C>T
NM_001002231.3:c.*1430C>T	NP_001002231.1:n.*1430C>T
NR_045762.2:n.2124C>T
NR_045763.2:n.2186C>T
NM_001256080.2:c.*1279C>T	NP_001243009.1:n.*1279C>T