Canonical Allele Identifier: CA2341114603

Gene: KLK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858232A= , CM000681.2:g.50858232A=	GRCh38
NC_000019.9:g.51361488A= , CM000681.1:g.51361488A=	GRCh37
NC_000019.8:g.56053300A=	NCBI36
NG_011653.1:g.8318A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.410A= MANE Select	ENSP00000314151.1:p.Lys137=
ENST00000326003.6:c.410A=	ENSP00000314151.1:p.Lys137=
ENST00000360617.7:c.410A=	ENSP00000353829.2:p.Lys137=
ENST00000422986.6:c.*66A=	ENSP00000393628.2:n.*66A=
ENST00000593997.5:c.410A=	ENSP00000472907.1:p.Lys137=
ENST00000595392.5:c.352+58A=	ENSP00000468912.1:n.352+58A=
ENST00000595952.5:c.281A=	ENSP00000471155.1:p.Lys94=
ENST00000596185.5:c.*518A=	ENSP00000471648.1:n.*518A=
ENST00000596333.1:n.445A=
ENST00000597286.5:c.299A=	ENSP00000470523.1:p.Lys100=
ENST00000597483.5:c.281A=	ENSP00000472411.1:p.Lys94=
ENST00000598145.1:c.394A=
ENST00000601349.5:n.1689A=
ENST00000601503.5:c.353A=	ENSP00000472213.1:p.Lys118=
ENST00000601812.1:n.842A=
ENST00000617027.4:c.353+57A=	ENSP00000483513.1:n.353+57A=
NM_001030047.1:c.410A=	NP_001025218.1:p.Lys137=
NM_001030048.1:c.281A=	NP_001025219.1:p.Lys94=
NM_001648.2:c.410A= MANE Select	NP_001639.1:p.Lys137=
XM_011526923.1:c.410A=	XP_011525225.1:p.Lys137=
XM_011526924.1:c.410A=	XP_011525226.1:p.Lys137=
XR_935817.1:n.445A=