Canonical Allele Identifier: CA508200853

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363365C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860109C>G , CM000681.2:g.50860109C>G	GRCh38
NC_000019.9:g.51363365C>G , CM000681.1:g.51363365C>G	GRCh37
NC_000019.8:g.56055177C>G	NCBI36
NG_011653.1:g.10195C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.768C>G MANE Select	ENSP00000314151.1:p.Thr256=
ENST00000326003.6:c.768C>G	ENSP00000314151.1:p.Thr256=
ENST00000360617.7:c.1210C>G	ENSP00000353829.2:n.1210C>G
ENST00000422986.6:c.*424C>G	ENSP00000393628.2:n.*424C>G
ENST00000595392.5:c.*269C>G	ENSP00000468912.1:n.*269C>G
ENST00000595952.5:c.639C>G	ENSP00000471155.1:p.Thr213=
ENST00000596333.1:n.946C>G
ENST00000598145.1:c.770C>G
ENST00000601349.5:n.2047C>G
ENST00000601812.1:n.1200C>G
ENST00000617027.4:c.645C>G	ENSP00000483513.1:p.Thr215=
NM_001030047.1:c.*493C>G	NP_001025218.1:n.*493C>G
NM_001030048.1:c.639C>G	NP_001025219.1:p.Thr213=
NM_001648.2:c.768C>G MANE Select	NP_001639.1:p.Thr256=
XM_011526923.1:c.786C>G	XP_011525225.1:p.Thr262=
XR_935817.1:n.1324+855C>G