Canonical Allele Identifier: CA9604616

Gene: KLK3

Linked Data

• dbSNP Id: rs776581784
• ExAC: 19:51363383 A / C
• MyVariant Identifiers: chr19:g.51363383A>C (hg19) ; chr19:g.50860127A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860127A>C , CM000681.2:g.50860127A>C	GRCh38
NC_000019.9:g.51363383A>C , CM000681.1:g.51363383A>C	GRCh37
NC_000019.8:g.56055195A>C	NCBI36
NG_011653.1:g.10213A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.786A>C MANE Select	ENSP00000314151.1:p.Ter262Cys
ENST00000326003.6:c.786A>C	ENSP00000314151.1:p.Ter262Cys
ENST00000360617.7:c.1228A>C	ENSP00000353829.2:n.1228A>C
ENST00000422986.6:c.*442A>C	ENSP00000393628.2:n.*442A>C
ENST00000595392.5:c.*287A>C	ENSP00000468912.1:n.*287A>C
ENST00000595952.5:c.657A>C	ENSP00000471155.1:p.Ter219Cys
ENST00000596333.1:n.964A>C
ENST00000598145.1:c.788A>C
ENST00000601349.5:n.2065A>C
ENST00000601812.1:n.1218A>C
ENST00000617027.4:c.663A>C	ENSP00000483513.1:p.Ter221Cys
NM_001030047.1:c.*511A>C	NP_001025218.1:n.*511A>C
NM_001030048.1:c.657A>C	NP_001025219.1:p.Ter219Cys
NM_001648.2:c.786A>C MANE Select	NP_001639.1:p.Ter262Cys
XM_011526923.1:c.804A>C	XP_011525225.1:p.Ter268Cys
XR_935817.1:n.1324+873A>C