Canonical Allele Identifier: CA2341114654

Gene: KLK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858353T= , CM000681.2:g.50858353T=	GRCh38
NC_000019.9:g.51361609T= , CM000681.1:g.51361609T=	GRCh37
NC_000019.8:g.56053421T=	NCBI36
NG_011653.1:g.8439T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.493+38T= MANE Select	ENSP00000314151.1:n.493+38T=
ENST00000326003.6:c.493+38T=	ENSP00000314151.1:n.493+38T=
ENST00000360617.7:c.493+38T=	ENSP00000353829.2:n.493+38T=
ENST00000422986.6:c.*149+38T=	ENSP00000393628.2:n.*149+38T=
ENST00000593997.5:c.493+38T=	ENSP00000472907.1:n.493+38T=
ENST00000595392.5:c.369+38T=	ENSP00000468912.1:n.369+38T=
ENST00000595952.5:c.364+38T=	ENSP00000471155.1:n.364+38T=
ENST00000596185.5:c.*601+38T=	ENSP00000471648.1:n.*601+38T=
ENST00000596333.1:n.566T=
ENST00000597286.5:c.382+38T=	ENSP00000470523.1:n.382+38T=
ENST00000597483.5:c.364+38T=	ENSP00000472411.1:n.364+38T=
ENST00000598145.1:c.495+20T=
ENST00000601349.5:n.1772+38T=
ENST00000601503.5:c.436+38T=	ENSP00000472213.1:n.436+38T=
ENST00000601812.1:n.925+38T=
ENST00000617027.4:c.370+38T=	ENSP00000483513.1:n.370+38T=
NM_001030047.1:c.493+38T=	NP_001025218.1:n.493+38T=
NM_001030048.1:c.364+38T=	NP_001025219.1:n.364+38T=
NM_001648.2:c.493+38T= MANE Select	NP_001639.1:n.493+38T=
XM_011526923.1:c.511+20T=	XP_011525225.1:n.511+20T=
XM_011526924.1:c.511+20T=	XP_011525226.1:n.511+20T=
XR_935817.1:n.528+38T=