Canonical Allele Identifier: CA2341115405

Gene: KLK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50859705T= , CM000681.2:g.50859705T=	GRCh38
NC_000019.9:g.51362961T= , CM000681.1:g.51362961T=	GRCh37
NC_000019.8:g.56054773T=	NCBI36
NG_011653.1:g.9791T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.631-267T= MANE Select	ENSP00000314151.1:n.631-267T=
ENST00000326003.6:c.631-267T=	ENSP00000314151.1:n.631-267T=
ENST00000360617.7:c.806T=	ENSP00000353829.2:n.806T=
ENST00000422986.6:c.*287-267T=	ENSP00000393628.2:n.*287-267T=
ENST00000595392.5:c.*132-267T=	ENSP00000468912.1:n.*132-267T=
ENST00000595952.5:c.502-267T=	ENSP00000471155.1:n.502-267T=
ENST00000596185.5:c.*739-267T=	ENSP00000471648.1:n.*739-267T=
ENST00000596333.1:n.809-267T=
ENST00000597483.5:c.*89T=	ENSP00000472411.1:n.*89T=
ENST00000598145.1:c.633-267T=
ENST00000601349.5:n.1910-267T=
ENST00000601812.1:n.1063-267T=
ENST00000617027.4:c.508-267T=	ENSP00000483513.1:n.508-267T=
NM_001030047.1:c.*89T=	NP_001025218.1:n.*89T=
NM_001030048.1:c.502-267T=	NP_001025219.1:n.502-267T=
NM_001648.2:c.631-267T= MANE Select	NP_001639.1:n.631-267T=
XM_011526923.1:c.649-267T=	XP_011525225.1:n.649-267T=
XM_011526924.1:c.*89T=	XP_011525226.1:n.*89T=
XR_935817.1:n.1324+451T=