Canonical Allele Identifier: CA508200851

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363359G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860103G>A , CM000681.2:g.50860103G>A	GRCh38
NC_000019.9:g.51363359G>A , CM000681.1:g.51363359G>A	GRCh37
NC_000019.8:g.56055171G>A	NCBI36
NG_011653.1:g.10189G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.762G>A MANE Select	ENSP00000314151.1:p.Lys254=
ENST00000326003.6:c.762G>A	ENSP00000314151.1:p.Lys254=
ENST00000360617.7:c.1204G>A	ENSP00000353829.2:n.1204G>A
ENST00000422986.6:c.*418G>A	ENSP00000393628.2:n.*418G>A
ENST00000595392.5:c.*263G>A	ENSP00000468912.1:n.*263G>A
ENST00000595952.5:c.633G>A	ENSP00000471155.1:p.Lys211=
ENST00000596333.1:n.940G>A
ENST00000598145.1:c.764G>A
ENST00000601349.5:n.2041G>A
ENST00000601812.1:n.1194G>A
ENST00000617027.4:c.639G>A	ENSP00000483513.1:p.Lys213=
NM_001030047.1:c.*487G>A	NP_001025218.1:n.*487G>A
NM_001030048.1:c.633G>A	NP_001025219.1:p.Lys211=
NM_001648.2:c.762G>A MANE Select	NP_001639.1:p.Lys254=
XM_011526923.1:c.780G>A	XP_011525225.1:p.Lys260=
XR_935817.1:n.1324+849G>A