Canonical Allele Identifier: CA2341114505

Gene: KLK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858036G= , CM000681.2:g.50858036G=	GRCh38
NC_000019.9:g.51361292G= , CM000681.1:g.51361292G=	GRCh37
NC_000019.8:g.56053104G=	NCBI36
NG_011653.1:g.8122G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.214G= MANE Select	ENSP00000314151.1:p.Val72=
ENST00000326003.6:c.214G=	ENSP00000314151.1:p.Val72=
ENST00000360617.7:c.214G=	ENSP00000353829.2:p.Val72=
ENST00000422986.6:c.214G=	ENSP00000393628.2:p.Val72=
ENST00000593997.5:c.214G=	ENSP00000472907.1:p.Val72=
ENST00000595392.5:c.214G=	ENSP00000468912.1:p.Val72=
ENST00000595952.5:c.207-122G=	ENSP00000471155.1:n.207-122G=
ENST00000596185.5:c.*322G=	ENSP00000471648.1:n.*322G=
ENST00000596333.1:n.249G=
ENST00000597286.5:c.103G=	ENSP00000470523.1:p.Val35=
ENST00000597483.5:c.207-122G=	ENSP00000472411.1:n.207-122G=
ENST00000598145.1:c.198G=
ENST00000601349.5:n.1493G=
ENST00000601503.5:c.157G=	ENSP00000472213.1:p.Val53=
ENST00000601812.1:n.646G=
ENST00000617027.4:c.214G=	ENSP00000483513.1:p.Val72=
NM_001030047.1:c.214G=	NP_001025218.1:p.Val72=
NM_001030048.1:c.207-122G=	NP_001025219.1:n.207-122G=
NM_001648.2:c.214G= MANE Select	NP_001639.1:p.Val72=
XM_011526923.1:c.214G=	XP_011525225.1:p.Val72=
XM_011526924.1:c.214G=	XP_011525226.1:p.Val72=
XR_935817.1:n.249G=