Canonical Allele Identifier: CA407025057

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363313G>A (hg19) ; chr19:g.50860057G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860057G>A , CM000681.2:g.50860057G>A	GRCh38
NC_000019.9:g.51363313G>A , CM000681.1:g.51363313G>A	GRCh37
NC_000019.8:g.56055125G>A	NCBI36
NG_011653.1:g.10143G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.716G>A MANE Select	ENSP00000314151.1:p.Arg239Lys
ENST00000326003.6:c.716G>A	ENSP00000314151.1:p.Arg239Lys
ENST00000360617.7:c.1158G>A	ENSP00000353829.2:n.1158G>A
ENST00000422986.6:c.*372G>A	ENSP00000393628.2:n.*372G>A
ENST00000595392.5:c.*217G>A	ENSP00000468912.1:n.*217G>A
ENST00000595952.5:c.587G>A	ENSP00000471155.1:p.Arg196Lys
ENST00000596333.1:n.894G>A
ENST00000598145.1:c.718G>A
ENST00000601349.5:n.1995G>A
ENST00000601812.1:n.1148G>A
ENST00000617027.4:c.593G>A	ENSP00000483513.1:p.Arg198Lys
NM_001030047.1:c.*441G>A	NP_001025218.1:n.*441G>A
NM_001030048.1:c.587G>A	NP_001025219.1:p.Arg196Lys
NM_001648.2:c.716G>A MANE Select	NP_001639.1:p.Arg239Lys
XM_011526923.1:c.734G>A	XP_011525225.1:p.Arg245Lys
XR_935817.1:n.1324+803G>A