Canonical Allele Identifier: CA2341114732

Gene: KLK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858501T= , CM000681.2:g.50858501T=	GRCh38
NC_000019.9:g.51361757T= , CM000681.1:g.51361757T=	GRCh37
NC_000019.8:g.56053569T=	NCBI36
NG_011653.1:g.8587T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001648.2:c.536T= MANE Select	NP_001639.1:p.Ile179=
ENST00000326003.7:c.536T= MANE Select	ENSP00000314151.1:p.Ile179=
NM_001030047.1:c.536T=	NP_001025218.1:p.Ile179=
NM_001030048.1:c.407T=	NP_001025219.1:p.Ile136=
ENST00000326003.6:c.536T=	ENSP00000314151.1:p.Ile179=
ENST00000360617.7:c.536T=	ENSP00000353829.2:p.Ile179=
ENST00000422986.6:c.*192T=	ENSP00000393628.2:n.*192T=
ENST00000593997.5:c.536T=	ENSP00000472907.1:p.Ile179=
ENST00000595392.5:c.*37T=	ENSP00000468912.1:n.*37T=
ENST00000595952.5:c.407T=	ENSP00000471155.1:p.Ile136=
ENST00000596185.5:c.*644T=	ENSP00000471648.1:n.*644T=
ENST00000596333.1:n.714T=
ENST00000597286.5:c.425T=	ENSP00000470523.1:p.Ile142=
ENST00000597483.5:c.407T=	ENSP00000472411.1:p.Ile136=
ENST00000598145.1:c.538T=
ENST00000601349.5:n.1815T=
ENST00000601503.5:c.479T=	ENSP00000472213.1:p.Ile160=
ENST00000601812.1:n.968T=
ENST00000617027.4:c.413T=	ENSP00000483513.1:p.Ile138=
XM_011526923.1:c.554T=	XP_011525225.1:p.Ile185=
XM_011526924.1:c.554T=	XP_011525226.1:p.Ile185=
XR_935817.1:n.571T=