Canonical Allele Identifier: CA407025286

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363381T>A (hg19) ; chr19:g.50860125T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860125T>A , CM000681.2:g.50860125T>A	GRCh38
NC_000019.9:g.51363381T>A , CM000681.1:g.51363381T>A	GRCh37
NC_000019.8:g.56055193T>A	NCBI36
NG_011653.1:g.10211T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.784T>A MANE Select	ENSP00000314151.1:p.Ter262Arg
ENST00000326003.6:c.784T>A	ENSP00000314151.1:p.Ter262Arg
ENST00000360617.7:c.1226T>A	ENSP00000353829.2:n.1226T>A
ENST00000422986.6:c.*440T>A	ENSP00000393628.2:n.*440T>A
ENST00000595392.5:c.*285T>A	ENSP00000468912.1:n.*285T>A
ENST00000595952.5:c.655T>A	ENSP00000471155.1:p.Ter219Arg
ENST00000596333.1:n.962T>A
ENST00000598145.1:c.786T>A
ENST00000601349.5:n.2063T>A
ENST00000601812.1:n.1216T>A
ENST00000617027.4:c.661T>A	ENSP00000483513.1:p.Ter221Arg
NM_001030047.1:c.*509T>A	NP_001025218.1:n.*509T>A
NM_001030048.1:c.655T>A	NP_001025219.1:p.Ter219Arg
NM_001648.2:c.784T>A MANE Select	NP_001639.1:p.Ter262Arg
XM_011526923.1:c.802T>A	XP_011525225.1:p.Ter268Arg
XR_935817.1:n.1324+871T>A