Canonical Allele Identifier: CA407025116

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363326C>G (hg19) ; chr19:g.50860070C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.729C>G MANE Select	ENSP00000314151.1:p.Tyr243Ter
ENST00000326003.6:c.729C>G	ENSP00000314151.1:p.Tyr243Ter
ENST00000360617.7:c.1171C>G	ENSP00000353829.2:n.1171C>G
ENST00000422986.6:c.*385C>G	ENSP00000393628.2:n.*385C>G
ENST00000595392.5:c.*230C>G	ENSP00000468912.1:n.*230C>G
ENST00000595952.5:c.600C>G	ENSP00000471155.1:p.Tyr200Ter
ENST00000596333.1:n.907C>G
ENST00000598145.1:c.731C>G
ENST00000601349.5:n.2008C>G
ENST00000601812.1:n.1161C>G
ENST00000617027.4:c.606C>G	ENSP00000483513.1:p.Tyr202Ter
NM_001030047.1:c.*454C>G	NP_001025218.1:n.*454C>G
NM_001030048.1:c.600C>G	NP_001025219.1:p.Tyr200Ter
NM_001648.2:c.729C>G MANE Select	NP_001639.1:p.Tyr243Ter
XM_011526923.1:c.747C>G	XP_011525225.1:p.Tyr249Ter
XR_935817.1:n.1324+816C>G