Canonical Allele Identifier: CA2341115537

Gene: KLK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50859994T= , CM000681.2:g.50859994T=	GRCh38
NC_000019.9:g.51363250T= , CM000681.1:g.51363250T=	GRCh37
NC_000019.8:g.56055062T=	NCBI36
NG_011653.1:g.10080T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.653T= MANE Select	ENSP00000314151.1:p.Val218=
ENST00000326003.6:c.653T=	ENSP00000314151.1:p.Val218=
ENST00000360617.7:c.1095T=	ENSP00000353829.2:n.1095T=
ENST00000422986.6:c.*309T=	ENSP00000393628.2:n.*309T=
ENST00000595392.5:c.*154T=	ENSP00000468912.1:n.*154T=
ENST00000595952.5:c.524T=	ENSP00000471155.1:p.Val175=
ENST00000596185.5:c.*761T=	ENSP00000471648.1:n.*761T=
ENST00000596333.1:n.831T=
ENST00000598145.1:c.655T=
ENST00000601349.5:n.1932T=
ENST00000601812.1:n.1085T=
ENST00000617027.4:c.530T=	ENSP00000483513.1:p.Val177=
NM_001030047.1:c.*378T=	NP_001025218.1:n.*378T=
NM_001030048.1:c.524T=	NP_001025219.1:p.Val175=
NM_001648.2:c.653T= MANE Select	NP_001639.1:p.Val218=
XM_011526923.1:c.671T=	XP_011525225.1:p.Val224=
XM_011526924.1:c.*378T=	XP_011525226.1:n.*378T=
XR_935817.1:n.1324+740T=