Canonical Allele Identifier: CA2341114396

Gene: KLK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50857810T= , CM000681.2:g.50857810T=	GRCh38
NC_000019.9:g.51361066T= , CM000681.1:g.51361066T=	GRCh37
NC_000019.8:g.56052878T=	NCBI36
NG_011653.1:g.7896T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.207-219T= MANE Select	ENSP00000314151.1:n.207-219T=
ENST00000326003.6:c.207-219T=	ENSP00000314151.1:n.207-219T=
ENST00000360617.7:c.207-219T=	ENSP00000353829.2:n.207-219T=
ENST00000422986.6:c.207-219T=	ENSP00000393628.2:n.207-219T=
ENST00000593997.5:c.207-219T=	ENSP00000472907.1:n.207-219T=
ENST00000595392.5:c.207-219T=	ENSP00000468912.1:n.207-219T=
ENST00000595952.5:c.207-348T=	ENSP00000471155.1:n.207-348T=
ENST00000596185.5:c.*315-219T=	ENSP00000471648.1:n.*315-219T=
ENST00000596333.1:n.242-219T=
ENST00000597286.5:c.96-219T=	ENSP00000470523.1:n.96-219T=
ENST00000597483.5:c.207-348T=	ENSP00000472411.1:n.207-348T=
ENST00000598145.1:c.191-219T=
ENST00000601349.5:n.1486-219T=
ENST00000601503.5:c.150-219T=	ENSP00000472213.1:n.150-219T=
ENST00000601812.1:n.420T=
ENST00000617027.4:c.207-219T=	ENSP00000483513.1:n.207-219T=
NM_001030047.1:c.207-219T=	NP_001025218.1:n.207-219T=
NM_001030048.1:c.207-348T=	NP_001025219.1:n.207-348T=
NM_001648.2:c.207-219T= MANE Select	NP_001639.1:n.207-219T=
XM_011526923.1:c.207-219T=	XP_011525225.1:n.207-219T=
XM_011526924.1:c.207-219T=	XP_011525226.1:n.207-219T=
XR_935817.1:n.242-219T=