Canonical Allele Identifier: CA2341114449

Gene: KLK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50857931T= , CM000681.2:g.50857931T=	GRCh38
NC_000019.9:g.51361187T= , CM000681.1:g.51361187T=	GRCh37
NC_000019.8:g.56052999T=	NCBI36
NG_011653.1:g.8017T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.207-98T= MANE Select	ENSP00000314151.1:n.207-98T=
ENST00000326003.6:c.207-98T=	ENSP00000314151.1:n.207-98T=
ENST00000360617.7:c.207-98T=	ENSP00000353829.2:n.207-98T=
ENST00000422986.6:c.207-98T=	ENSP00000393628.2:n.207-98T=
ENST00000593997.5:c.207-98T=	ENSP00000472907.1:n.207-98T=
ENST00000595392.5:c.207-98T=	ENSP00000468912.1:n.207-98T=
ENST00000595952.5:c.207-227T=	ENSP00000471155.1:n.207-227T=
ENST00000596185.5:c.*315-98T=	ENSP00000471648.1:n.*315-98T=
ENST00000596333.1:n.242-98T=
ENST00000597286.5:c.96-98T=	ENSP00000470523.1:n.96-98T=
ENST00000597483.5:c.207-227T=	ENSP00000472411.1:n.207-227T=
ENST00000598145.1:c.191-98T=
ENST00000601349.5:n.1486-98T=
ENST00000601503.5:c.150-98T=	ENSP00000472213.1:n.150-98T=
ENST00000601812.1:n.541T=
ENST00000617027.4:c.207-98T=	ENSP00000483513.1:n.207-98T=
NM_001030047.1:c.207-98T=	NP_001025218.1:n.207-98T=
NM_001030048.1:c.207-227T=	NP_001025219.1:n.207-227T=
NM_001648.2:c.207-98T= MANE Select	NP_001639.1:n.207-98T=
XM_011526923.1:c.207-98T=	XP_011525225.1:n.207-98T=
XM_011526924.1:c.207-98T=	XP_011525226.1:n.207-98T=
XR_935817.1:n.242-98T=