Canonical Allele Identifier: CA2341114624

Gene: KLK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858293G= , CM000681.2:g.50858293G=	GRCh38
NC_000019.9:g.51361549G= , CM000681.1:g.51361549G=	GRCh37
NC_000019.8:g.56053361G=	NCBI36
NG_011653.1:g.8379G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.471G= MANE Select	ENSP00000314151.1:p.Trp157=
ENST00000326003.6:c.471G=	ENSP00000314151.1:p.Trp157=
ENST00000360617.7:c.471G=	ENSP00000353829.2:p.Trp157=
ENST00000422986.6:c.*127G=	ENSP00000393628.2:n.*127G=
ENST00000593997.5:c.471G=	ENSP00000472907.1:p.Trp157=
ENST00000595392.5:c.353-6G=	ENSP00000468912.1:n.353-6G=
ENST00000595952.5:c.342G=	ENSP00000471155.1:p.Trp114=
ENST00000596185.5:c.*579G=	ENSP00000471648.1:n.*579G=
ENST00000596333.1:n.506G=
ENST00000597286.5:c.360G=	ENSP00000470523.1:p.Trp120=
ENST00000597483.5:c.342G=	ENSP00000472411.1:p.Trp114=
ENST00000598145.1:c.455G=
ENST00000601349.5:n.1750G=
ENST00000601503.5:c.414G=	ENSP00000472213.1:p.Trp138=
ENST00000601812.1:n.903G=
ENST00000617027.4:c.354-6G=	ENSP00000483513.1:n.354-6G=
NM_001030047.1:c.471G=	NP_001025218.1:p.Trp157=
NM_001030048.1:c.342G=	NP_001025219.1:p.Trp114=
NM_001648.2:c.471G= MANE Select	NP_001639.1:p.Trp157=
XM_011526923.1:c.471G=	XP_011525225.1:p.Trp157=
XM_011526924.1:c.471G=	XP_011525226.1:p.Trp157=
XR_935817.1:n.506G=