Canonical Allele Identifier: CA407022774

Gene: KLK3

Linked Data

• dbSNP Id: rs1402450333
• gnomAD v2: 19-51361533-G-A
• gnomAD v4: 19-50858277-G-A
• MyVariant Identifiers: chr19:g.51361533G>A (hg19) ; chr19:g.50858277G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858277G>A , CM000681.2:g.50858277G>A	GRCh38
NC_000019.9:g.51361533G>A , CM000681.1:g.51361533G>A	GRCh37
NC_000019.8:g.56053345G>A	NCBI36
NG_011653.1:g.8363G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.455G>A MANE Select	ENSP00000314151.1:p.Cys152Tyr
ENST00000326003.6:c.455G>A	ENSP00000314151.1:p.Cys152Tyr
ENST00000360617.7:c.455G>A	ENSP00000353829.2:p.Cys152Tyr
ENST00000422986.6:c.*111G>A	ENSP00000393628.2:n.*111G>A
ENST00000593997.5:c.455G>A	ENSP00000472907.1:p.Cys152Tyr
ENST00000595392.5:c.353-22G>A	ENSP00000468912.1:n.353-22G>A
ENST00000595952.5:c.326G>A	ENSP00000471155.1:p.Cys109Tyr
ENST00000596185.5:c.*563G>A	ENSP00000471648.1:n.*563G>A
ENST00000596333.1:n.490G>A
ENST00000597286.5:c.344G>A	ENSP00000470523.1:p.Cys115Tyr
ENST00000597483.5:c.326G>A	ENSP00000472411.1:p.Cys109Tyr
ENST00000598145.1:c.439G>A
ENST00000601349.5:n.1734G>A
ENST00000601503.5:c.398G>A	ENSP00000472213.1:p.Cys133Tyr
ENST00000601812.1:n.887G>A
ENST00000617027.4:c.354-22G>A	ENSP00000483513.1:n.354-22G>A
NM_001030047.1:c.455G>A	NP_001025218.1:p.Cys152Tyr
NM_001030048.1:c.326G>A	NP_001025219.1:p.Cys109Tyr
NM_001648.2:c.455G>A MANE Select	NP_001639.1:p.Cys152Tyr
XM_011526923.1:c.455G>A	XP_011525225.1:p.Cys152Tyr
XM_011526924.1:c.455G>A	XP_011525226.1:p.Cys152Tyr
XR_935817.1:n.490G>A