Canonical Allele Identifier: CA407024819

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363228G>T (hg19) ; chr19:g.50859972G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50859972G>T , CM000681.2:g.50859972G>T	GRCh38
NC_000019.9:g.51363228G>T , CM000681.1:g.51363228G>T	GRCh37
NC_000019.8:g.56055040G>T	NCBI36
NG_011653.1:g.10058G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.631G>T MANE Select	ENSP00000314151.1:p.Gly211Cys
ENST00000326003.6:c.631G>T	ENSP00000314151.1:p.Gly211Cys
ENST00000360617.7:c.1073G>T	ENSP00000353829.2:n.1073G>T
ENST00000422986.6:c.*287G>T	ENSP00000393628.2:n.*287G>T
ENST00000595392.5:c.*132G>T	ENSP00000468912.1:n.*132G>T
ENST00000595952.5:c.502G>T	ENSP00000471155.1:p.Gly168Cys
ENST00000596185.5:c.*739G>T	ENSP00000471648.1:n.*739G>T
ENST00000596333.1:n.809G>T
ENST00000598145.1:c.633G>T
ENST00000601349.5:n.1910G>T
ENST00000601812.1:n.1063G>T
ENST00000617027.4:c.508G>T	ENSP00000483513.1:p.Gly170Cys
NM_001030047.1:c.*356G>T	NP_001025218.1:n.*356G>T
NM_001030048.1:c.502G>T	NP_001025219.1:p.Gly168Cys
NM_001648.2:c.631G>T MANE Select	NP_001639.1:p.Gly211Cys
XM_011526923.1:c.649G>T	XP_011525225.1:p.Gly217Cys
XM_011526924.1:c.*356G>T	XP_011525226.1:n.*356G>T
XR_935817.1:n.1324+718G>T