Canonical Allele Identifier: CA508200863

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363380C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860124C>G , CM000681.2:g.50860124C>G	GRCh38
NC_000019.9:g.51363380C>G , CM000681.1:g.51363380C>G	GRCh37
NC_000019.8:g.56055192C>G	NCBI36
NG_011653.1:g.10210C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.783C>G MANE Select	ENSP00000314151.1:p.Pro261=
ENST00000326003.6:c.783C>G	ENSP00000314151.1:p.Pro261=
ENST00000360617.7:c.1225C>G	ENSP00000353829.2:n.1225C>G
ENST00000422986.6:c.*439C>G	ENSP00000393628.2:n.*439C>G
ENST00000595392.5:c.*284C>G	ENSP00000468912.1:n.*284C>G
ENST00000595952.5:c.654C>G	ENSP00000471155.1:p.Pro218=
ENST00000596333.1:n.961C>G
ENST00000598145.1:c.785C>G
ENST00000601349.5:n.2062C>G
ENST00000601812.1:n.1215C>G
ENST00000617027.4:c.660C>G	ENSP00000483513.1:p.Pro220=
NM_001030047.1:c.*508C>G	NP_001025218.1:n.*508C>G
NM_001030048.1:c.654C>G	NP_001025219.1:p.Pro218=
NM_001648.2:c.783C>G MANE Select	NP_001639.1:p.Pro261=
XM_011526923.1:c.801C>G	XP_011525225.1:p.Pro267=
XR_935817.1:n.1324+870C>G