Canonical Allele Identifier: CA407025056

Gene: KLK3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.716G>C MANE Select	ENSP00000314151.1:p.Arg239Thr
ENST00000326003.6:c.716G>C	ENSP00000314151.1:p.Arg239Thr
ENST00000360617.7:c.1158G>C	ENSP00000353829.2:n.1158G>C
ENST00000422986.6:c.*372G>C	ENSP00000393628.2:n.*372G>C
ENST00000595392.5:c.*217G>C	ENSP00000468912.1:n.*217G>C
ENST00000595952.5:c.587G>C	ENSP00000471155.1:p.Arg196Thr
ENST00000596333.1:n.894G>C
ENST00000598145.1:c.718G>C
ENST00000601349.5:n.1995G>C
ENST00000601812.1:n.1148G>C
ENST00000617027.4:c.593G>C	ENSP00000483513.1:p.Arg198Thr
NM_001030047.1:c.*441G>C	NP_001025218.1:n.*441G>C
NM_001030048.1:c.587G>C	NP_001025219.1:p.Arg196Thr
NM_001648.2:c.716G>C MANE Select	NP_001639.1:p.Arg239Thr
XM_011526923.1:c.734G>C	XP_011525225.1:p.Arg245Thr
XR_935817.1:n.1324+803G>C