Canonical Allele Identifier: CA407024991

Gene: KLK3

Linked Data

• dbSNP Id: rs1599996667
• MyVariant Identifiers: chr19:g.51363298G>A (hg19) ; chr19:g.50860042G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860042G>A , CM000681.2:g.50860042G>A	GRCh38
NC_000019.9:g.51363298G>A , CM000681.1:g.51363298G>A	GRCh37
NC_000019.8:g.56055110G>A	NCBI36
NG_011653.1:g.10128G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.701G>A MANE Select	ENSP00000314151.1:p.Cys234Tyr
ENST00000326003.6:c.701G>A	ENSP00000314151.1:p.Cys234Tyr
ENST00000360617.7:c.1143G>A	ENSP00000353829.2:n.1143G>A
ENST00000422986.6:c.*357G>A	ENSP00000393628.2:n.*357G>A
ENST00000595392.5:c.*202G>A	ENSP00000468912.1:n.*202G>A
ENST00000595952.5:c.572G>A	ENSP00000471155.1:p.Cys191Tyr
ENST00000596333.1:n.879G>A
ENST00000598145.1:c.703G>A
ENST00000601349.5:n.1980G>A
ENST00000601812.1:n.1133G>A
ENST00000617027.4:c.578G>A	ENSP00000483513.1:p.Cys193Tyr
NM_001030047.1:c.*426G>A	NP_001025218.1:n.*426G>A
NM_001030048.1:c.572G>A	NP_001025219.1:p.Cys191Tyr
NM_001648.2:c.701G>A MANE Select	NP_001639.1:p.Cys234Tyr
XM_011526923.1:c.719G>A	XP_011525225.1:p.Cys240Tyr
XR_935817.1:n.1324+788G>A