Canonical Allele Identifier: CA508200833

Gene: KLK3

Linked Data

• dbSNP Id: rs2090175334
• COSMIC: COSM3773121
• MyVariant Identifiers: chr19:g.51363326C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860070C>T , CM000681.2:g.50860070C>T	GRCh38
NC_000019.9:g.51363326C>T , CM000681.1:g.51363326C>T	GRCh37
NC_000019.8:g.56055138C>T	NCBI36
NG_011653.1:g.10156C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.729C>T MANE Select	ENSP00000314151.1:p.Tyr243=
ENST00000326003.6:c.729C>T	ENSP00000314151.1:p.Tyr243=
ENST00000360617.7:c.1171C>T	ENSP00000353829.2:n.1171C>T
ENST00000422986.6:c.*385C>T	ENSP00000393628.2:n.*385C>T
ENST00000595392.5:c.*230C>T	ENSP00000468912.1:n.*230C>T
ENST00000595952.5:c.600C>T	ENSP00000471155.1:p.Tyr200=
ENST00000596333.1:n.907C>T
ENST00000598145.1:c.731C>T
ENST00000601349.5:n.2008C>T
ENST00000601812.1:n.1161C>T
ENST00000617027.4:c.606C>T	ENSP00000483513.1:p.Tyr202=
NM_001030047.1:c.*454C>T	NP_001025218.1:n.*454C>T
NM_001030048.1:c.600C>T	NP_001025219.1:p.Tyr200=
NM_001648.2:c.729C>T MANE Select	NP_001639.1:p.Tyr243=
XM_011526923.1:c.747C>T	XP_011525225.1:p.Tyr249=
XR_935817.1:n.1324+816C>T