Canonical Allele Identifier: CA407022729

Gene: KLK3

Linked Data

• gnomAD v4: 19-50858255-G-A
• MyVariant Identifiers: chr19:g.51361511G>A (hg19) ; chr19:g.50858255G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858255G>A , CM000681.2:g.50858255G>A	GRCh38
NC_000019.9:g.51361511G>A , CM000681.1:g.51361511G>A	GRCh37
NC_000019.8:g.56053323G>A	NCBI36
NG_011653.1:g.8341G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.433G>A MANE Select	ENSP00000314151.1:p.Glu145Lys
ENST00000326003.6:c.433G>A	ENSP00000314151.1:p.Glu145Lys
ENST00000360617.7:c.433G>A	ENSP00000353829.2:p.Glu145Lys
ENST00000422986.6:c.*89G>A	ENSP00000393628.2:n.*89G>A
ENST00000593997.5:c.433G>A	ENSP00000472907.1:p.Glu145Lys
ENST00000595392.5:c.353-44G>A	ENSP00000468912.1:n.353-44G>A
ENST00000595952.5:c.304G>A	ENSP00000471155.1:p.Glu102Lys
ENST00000596185.5:c.*541G>A	ENSP00000471648.1:n.*541G>A
ENST00000596333.1:n.468G>A
ENST00000597286.5:c.322G>A	ENSP00000470523.1:p.Glu108Lys
ENST00000597483.5:c.304G>A	ENSP00000472411.1:p.Glu102Lys
ENST00000598145.1:c.417G>A
ENST00000601349.5:n.1712G>A
ENST00000601503.5:c.376G>A	ENSP00000472213.1:p.Glu126Lys
ENST00000601812.1:n.865G>A
ENST00000617027.4:c.354-44G>A	ENSP00000483513.1:n.354-44G>A
NM_001030047.1:c.433G>A	NP_001025218.1:p.Glu145Lys
NM_001030048.1:c.304G>A	NP_001025219.1:p.Glu102Lys
NM_001648.2:c.433G>A MANE Select	NP_001639.1:p.Glu145Lys
XM_011526923.1:c.433G>A	XP_011525225.1:p.Glu145Lys
XM_011526924.1:c.433G>A	XP_011525226.1:p.Glu145Lys
XR_935817.1:n.468G>A