Canonical Allele Identifier: CA407025094

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363322T>A (hg19) ; chr19:g.50860066T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860066T>A , CM000681.2:g.50860066T>A	GRCh38
NC_000019.9:g.51363322T>A , CM000681.1:g.51363322T>A	GRCh37
NC_000019.8:g.56055134T>A	NCBI36
NG_011653.1:g.10152T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.725T>A MANE Select	ENSP00000314151.1:p.Leu242Gln
ENST00000326003.6:c.725T>A	ENSP00000314151.1:p.Leu242Gln
ENST00000360617.7:c.1167T>A	ENSP00000353829.2:n.1167T>A
ENST00000422986.6:c.*381T>A	ENSP00000393628.2:n.*381T>A
ENST00000595392.5:c.*226T>A	ENSP00000468912.1:n.*226T>A
ENST00000595952.5:c.596T>A	ENSP00000471155.1:p.Leu199Gln
ENST00000596333.1:n.903T>A
ENST00000598145.1:c.727T>A
ENST00000601349.5:n.2004T>A
ENST00000601812.1:n.1157T>A
ENST00000617027.4:c.602T>A	ENSP00000483513.1:p.Leu201Gln
NM_001030047.1:c.*450T>A	NP_001025218.1:n.*450T>A
NM_001030048.1:c.596T>A	NP_001025219.1:p.Leu199Gln
NM_001648.2:c.725T>A MANE Select	NP_001639.1:p.Leu242Gln
XM_011526923.1:c.743T>A	XP_011525225.1:p.Leu248Gln
XR_935817.1:n.1324+812T>A