Canonical Allele Identifier: CA407025105

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363324T>G (hg19) ; chr19:g.50860068T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860068T>G , CM000681.2:g.50860068T>G	GRCh38
NC_000019.9:g.51363324T>G , CM000681.1:g.51363324T>G	GRCh37
NC_000019.8:g.56055136T>G	NCBI36
NG_011653.1:g.10154T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.727T>G MANE Select	ENSP00000314151.1:p.Tyr243Asp
ENST00000326003.6:c.727T>G	ENSP00000314151.1:p.Tyr243Asp
ENST00000360617.7:c.1169T>G	ENSP00000353829.2:n.1169T>G
ENST00000422986.6:c.*383T>G	ENSP00000393628.2:n.*383T>G
ENST00000595392.5:c.*228T>G	ENSP00000468912.1:n.*228T>G
ENST00000595952.5:c.598T>G	ENSP00000471155.1:p.Tyr200Asp
ENST00000596333.1:n.905T>G
ENST00000598145.1:c.729T>G
ENST00000601349.5:n.2006T>G
ENST00000601812.1:n.1159T>G
ENST00000617027.4:c.604T>G	ENSP00000483513.1:p.Tyr202Asp
NM_001030047.1:c.*452T>G	NP_001025218.1:n.*452T>G
NM_001030048.1:c.598T>G	NP_001025219.1:p.Tyr200Asp
NM_001648.2:c.727T>G MANE Select	NP_001639.1:p.Tyr243Asp
XM_011526923.1:c.745T>G	XP_011525225.1:p.Tyr249Asp
XR_935817.1:n.1324+814T>G