Canonical Allele Identifier: CA407025098

Gene: KLK3

Linked Data

• gnomAD v4: 19-50860066-T-G
• MyVariant Identifiers: chr19:g.51363322T>G (hg19) ; chr19:g.50860066T>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.725T>G MANE Select	ENSP00000314151.1:p.Leu242Arg
ENST00000326003.6:c.725T>G	ENSP00000314151.1:p.Leu242Arg
ENST00000360617.7:c.1167T>G	ENSP00000353829.2:n.1167T>G
ENST00000422986.6:c.*381T>G	ENSP00000393628.2:n.*381T>G
ENST00000595392.5:c.*226T>G	ENSP00000468912.1:n.*226T>G
ENST00000595952.5:c.596T>G	ENSP00000471155.1:p.Leu199Arg
ENST00000596333.1:n.903T>G
ENST00000598145.1:c.727T>G
ENST00000601349.5:n.2004T>G
ENST00000601812.1:n.1157T>G
ENST00000617027.4:c.602T>G	ENSP00000483513.1:p.Leu201Arg
NM_001030047.1:c.*450T>G	NP_001025218.1:n.*450T>G
NM_001030048.1:c.596T>G	NP_001025219.1:p.Leu199Arg
NM_001648.2:c.725T>G MANE Select	NP_001639.1:p.Leu242Arg
XM_011526923.1:c.743T>G	XP_011525225.1:p.Leu248Arg
XR_935817.1:n.1324+812T>G