Canonical Allele Identifier: CA407025153

Gene: KLK3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.739G>C MANE Select	ENSP00000314151.1:p.Val247Leu
ENST00000326003.6:c.739G>C	ENSP00000314151.1:p.Val247Leu
ENST00000360617.7:c.1181G>C	ENSP00000353829.2:n.1181G>C
ENST00000422986.6:c.*395G>C	ENSP00000393628.2:n.*395G>C
ENST00000595392.5:c.*240G>C	ENSP00000468912.1:n.*240G>C
ENST00000595952.5:c.610G>C	ENSP00000471155.1:p.Val204Leu
ENST00000596333.1:n.917G>C
ENST00000598145.1:c.741G>C
ENST00000601349.5:n.2018G>C
ENST00000601812.1:n.1171G>C
ENST00000617027.4:c.616G>C	ENSP00000483513.1:p.Val206Leu
NM_001030047.1:c.*464G>C	NP_001025218.1:n.*464G>C
NM_001030048.1:c.610G>C	NP_001025219.1:p.Val204Leu
NM_001648.2:c.739G>C MANE Select	NP_001639.1:p.Val247Leu
XM_011526923.1:c.757G>C	XP_011525225.1:p.Val253Leu
XR_935817.1:n.1324+826G>C