Canonical Allele Identifier: CA2341115407

Gene: KLK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50859706C= , CM000681.2:g.50859706C=	GRCh38
NC_000019.9:g.51362962C= , CM000681.1:g.51362962C=	GRCh37
NC_000019.8:g.56054774C=	NCBI36
NG_011653.1:g.9792C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.631-266C= MANE Select	ENSP00000314151.1:n.631-266C=
ENST00000326003.6:c.631-266C=	ENSP00000314151.1:n.631-266C=
ENST00000360617.7:c.807C=	ENSP00000353829.2:n.807C=
ENST00000422986.6:c.*287-266C=	ENSP00000393628.2:n.*287-266C=
ENST00000595392.5:c.*132-266C=	ENSP00000468912.1:n.*132-266C=
ENST00000595952.5:c.502-266C=	ENSP00000471155.1:n.502-266C=
ENST00000596185.5:c.*739-266C=	ENSP00000471648.1:n.*739-266C=
ENST00000596333.1:n.809-266C=
ENST00000597483.5:c.*90C=	ENSP00000472411.1:n.*90C=
ENST00000598145.1:c.633-266C=
ENST00000601349.5:n.1910-266C=
ENST00000601812.1:n.1063-266C=
ENST00000617027.4:c.508-266C=	ENSP00000483513.1:n.508-266C=
NM_001030047.1:c.*90C=	NP_001025218.1:n.*90C=
NM_001030048.1:c.502-266C=	NP_001025219.1:n.502-266C=
NM_001648.2:c.631-266C= MANE Select	NP_001639.1:n.631-266C=
XM_011526923.1:c.649-266C=	XP_011525225.1:n.649-266C=
XM_011526924.1:c.*90C=	XP_011525226.1:n.*90C=
XR_935817.1:n.1324+452C=