Canonical Allele Identifier: CA2341114592

Gene: KLK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858216C= , CM000681.2:g.50858216C=	GRCh38
NC_000019.9:g.51361472C= , CM000681.1:g.51361472C=	GRCh37
NC_000019.8:g.56053284C=	NCBI36
NG_011653.1:g.8302C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001648.2:c.394C= MANE Select	NP_001639.1:p.Leu132=
ENST00000326003.7:c.394C= MANE Select	ENSP00000314151.1:p.Leu132=
NM_001030047.1:c.394C=	NP_001025218.1:p.Leu132=
NM_001030048.1:c.265C=	NP_001025219.1:p.Leu89=
ENST00000326003.6:c.394C=	ENSP00000314151.1:p.Leu132=
ENST00000360617.7:c.394C=	ENSP00000353829.2:p.Leu132=
ENST00000422986.6:c.*50C=	ENSP00000393628.2:n.*50C=
ENST00000593997.5:c.394C=	ENSP00000472907.1:p.Leu132=
ENST00000595392.5:c.352+42C=	ENSP00000468912.1:n.352+42C=
ENST00000595952.5:c.265C=	ENSP00000471155.1:p.Leu89=
ENST00000596185.5:c.*502C=	ENSP00000471648.1:n.*502C=
ENST00000596333.1:n.429C=
ENST00000597286.5:c.283C=	ENSP00000470523.1:p.Leu95=
ENST00000597483.5:c.265C=	ENSP00000472411.1:p.Leu89=
ENST00000598145.1:c.378C=
ENST00000601349.5:n.1673C=
ENST00000601503.5:c.337C=	ENSP00000472213.1:p.Leu113=
ENST00000601812.1:n.826C=
ENST00000617027.4:c.353+41C=	ENSP00000483513.1:n.353+41C=
XM_011526923.1:c.394C=	XP_011525225.1:p.Leu132=
XM_011526924.1:c.394C=	XP_011525226.1:p.Leu132=
XR_935817.1:n.429C=