Canonical Allele Identifier: CA9604610

Gene: KLK3

Linked Data

• dbSNP Id: rs200006942
• ExAC: 19:51363369 G / A
• gnomAD v2: 19-51363369-G-A
• gnomAD v3: 19-50860113-G-A
• gnomAD v4: 19-50860113-G-A
• MyVariant Identifiers: chr19:g.51363369G>A (hg19) ; chr19:g.50860113G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860113G>A , CM000681.2:g.50860113G>A	GRCh38
NC_000019.9:g.51363369G>A , CM000681.1:g.51363369G>A	GRCh37
NC_000019.8:g.56055181G>A	NCBI36
NG_011653.1:g.10199G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.772G>A MANE Select	ENSP00000314151.1:p.Val258Met
ENST00000326003.6:c.772G>A	ENSP00000314151.1:p.Val258Met
ENST00000360617.7:c.1214G>A	ENSP00000353829.2:n.1214G>A
ENST00000422986.6:c.*428G>A	ENSP00000393628.2:n.*428G>A
ENST00000595392.5:c.*273G>A	ENSP00000468912.1:n.*273G>A
ENST00000595952.5:c.643G>A	ENSP00000471155.1:p.Val215Met
ENST00000596333.1:n.950G>A
ENST00000598145.1:c.774G>A
ENST00000601349.5:n.2051G>A
ENST00000601812.1:n.1204G>A
ENST00000617027.4:c.649G>A	ENSP00000483513.1:p.Val217Met
NM_001030047.1:c.*497G>A	NP_001025218.1:n.*497G>A
NM_001030048.1:c.643G>A	NP_001025219.1:p.Val215Met
NM_001648.2:c.772G>A MANE Select	NP_001639.1:p.Val258Met
XM_011526923.1:c.790G>A	XP_011525225.1:p.Val264Met
XR_935817.1:n.1324+859G>A