Canonical Allele Identifier: CA407025189

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363353G>C (hg19) ; chr19:g.50860097G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860097G>C , CM000681.2:g.50860097G>C	GRCh38
NC_000019.9:g.51363353G>C , CM000681.1:g.51363353G>C	GRCh37
NC_000019.8:g.56055165G>C	NCBI36
NG_011653.1:g.10183G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.756G>C MANE Select	ENSP00000314151.1:p.Trp252Cys
ENST00000326003.6:c.756G>C	ENSP00000314151.1:p.Trp252Cys
ENST00000360617.7:c.1198G>C	ENSP00000353829.2:n.1198G>C
ENST00000422986.6:c.*412G>C	ENSP00000393628.2:n.*412G>C
ENST00000595392.5:c.*257G>C	ENSP00000468912.1:n.*257G>C
ENST00000595952.5:c.627G>C	ENSP00000471155.1:p.Trp209Cys
ENST00000596333.1:n.934G>C
ENST00000598145.1:c.758G>C
ENST00000601349.5:n.2035G>C
ENST00000601812.1:n.1188G>C
ENST00000617027.4:c.633G>C	ENSP00000483513.1:p.Trp211Cys
NM_001030047.1:c.*481G>C	NP_001025218.1:n.*481G>C
NM_001030048.1:c.627G>C	NP_001025219.1:p.Trp209Cys
NM_001648.2:c.756G>C MANE Select	NP_001639.1:p.Trp252Cys
XM_011526923.1:c.774G>C	XP_011525225.1:p.Trp258Cys
XR_935817.1:n.1324+843G>C