Canonical Allele Identifier: CA407025165

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363342T>G (hg19) ; chr19:g.50860086T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860086T>G , CM000681.2:g.50860086T>G	GRCh38
NC_000019.9:g.51363342T>G , CM000681.1:g.51363342T>G	GRCh37
NC_000019.8:g.56055154T>G	NCBI36
NG_011653.1:g.10172T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.745T>G MANE Select	ENSP00000314151.1:p.Tyr249Asp
ENST00000326003.6:c.745T>G	ENSP00000314151.1:p.Tyr249Asp
ENST00000360617.7:c.1187T>G	ENSP00000353829.2:n.1187T>G
ENST00000422986.6:c.*401T>G	ENSP00000393628.2:n.*401T>G
ENST00000595392.5:c.*246T>G	ENSP00000468912.1:n.*246T>G
ENST00000595952.5:c.616T>G	ENSP00000471155.1:p.Tyr206Asp
ENST00000596333.1:n.923T>G
ENST00000598145.1:c.747T>G
ENST00000601349.5:n.2024T>G
ENST00000601812.1:n.1177T>G
ENST00000617027.4:c.622T>G	ENSP00000483513.1:p.Tyr208Asp
NM_001030047.1:c.*470T>G	NP_001025218.1:n.*470T>G
NM_001030048.1:c.616T>G	NP_001025219.1:p.Tyr206Asp
NM_001648.2:c.745T>G MANE Select	NP_001639.1:p.Tyr249Asp
XM_011526923.1:c.763T>G	XP_011525225.1:p.Tyr255Asp
XR_935817.1:n.1324+832T>G