Canonical Allele Identifier: CA407025152

Gene: KLK3

Linked Data

• COSMIC: COSM6055191
• MyVariant Identifiers: chr19:g.51363336G>A (hg19) ; chr19:g.50860080G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860080G>A , CM000681.2:g.50860080G>A	GRCh38
NC_000019.9:g.51363336G>A , CM000681.1:g.51363336G>A	GRCh37
NC_000019.8:g.56055148G>A	NCBI36
NG_011653.1:g.10166G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.739G>A MANE Select	ENSP00000314151.1:p.Val247Met
ENST00000326003.6:c.739G>A	ENSP00000314151.1:p.Val247Met
ENST00000360617.7:c.1181G>A	ENSP00000353829.2:n.1181G>A
ENST00000422986.6:c.*395G>A	ENSP00000393628.2:n.*395G>A
ENST00000595392.5:c.*240G>A	ENSP00000468912.1:n.*240G>A
ENST00000595952.5:c.610G>A	ENSP00000471155.1:p.Val204Met
ENST00000596333.1:n.917G>A
ENST00000598145.1:c.741G>A
ENST00000601349.5:n.2018G>A
ENST00000601812.1:n.1171G>A
ENST00000617027.4:c.616G>A	ENSP00000483513.1:p.Val206Met
NM_001030047.1:c.*464G>A	NP_001025218.1:n.*464G>A
NM_001030048.1:c.610G>A	NP_001025219.1:p.Val204Met
NM_001648.2:c.739G>A MANE Select	NP_001639.1:p.Val247Met
XM_011526923.1:c.757G>A	XP_011525225.1:p.Val253Met
XR_935817.1:n.1324+826G>A