Canonical Allele Identifier: CA309633998

Gene: KLK3

Linked Data

• dbSNP Id: rs1802720
• MyVariant Identifiers: chr19:g.51363342T>C (hg19) ; chr19:g.50860086T>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.745T>C MANE Select	ENSP00000314151.1:p.Tyr249His
ENST00000326003.6:c.745T>C	ENSP00000314151.1:p.Tyr249His
ENST00000360617.7:c.1187T>C	ENSP00000353829.2:n.1187T>C
ENST00000422986.6:c.*401T>C	ENSP00000393628.2:n.*401T>C
ENST00000595392.5:c.*246T>C	ENSP00000468912.1:n.*246T>C
ENST00000595952.5:c.616T>C	ENSP00000471155.1:p.Tyr206His
ENST00000596333.1:n.923T>C
ENST00000598145.1:c.747T>C
ENST00000601349.5:n.2024T>C
ENST00000601812.1:n.1177T>C
ENST00000617027.4:c.622T>C	ENSP00000483513.1:p.Tyr208His
NM_001030047.1:c.*470T>C	NP_001025218.1:n.*470T>C
NM_001030048.1:c.616T>C	NP_001025219.1:p.Tyr206His
NM_001648.2:c.745T>C MANE Select	NP_001639.1:p.Tyr249His
XM_011526923.1:c.763T>C	XP_011525225.1:p.Tyr255His
XR_935817.1:n.1324+832T>C