Canonical Allele Identifier: CA2341115412

Gene: KLK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50859723G= , CM000681.2:g.50859723G=	GRCh38
NC_000019.9:g.51362979G= , CM000681.1:g.51362979G=	GRCh37
NC_000019.8:g.56054791G=	NCBI36
NG_011653.1:g.9809G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.631-249G= MANE Select	ENSP00000314151.1:n.631-249G=
ENST00000326003.6:c.631-249G=	ENSP00000314151.1:n.631-249G=
ENST00000360617.7:c.824G=	ENSP00000353829.2:n.824G=
ENST00000422986.6:c.*287-249G=	ENSP00000393628.2:n.*287-249G=
ENST00000595392.5:c.*132-249G=	ENSP00000468912.1:n.*132-249G=
ENST00000595952.5:c.502-249G=	ENSP00000471155.1:n.502-249G=
ENST00000596185.5:c.*739-249G=	ENSP00000471648.1:n.*739-249G=
ENST00000596333.1:n.809-249G=
ENST00000597483.5:c.*107G=	ENSP00000472411.1:n.*107G=
ENST00000598145.1:c.633-249G=
ENST00000601349.5:n.1910-249G=
ENST00000601812.1:n.1063-249G=
ENST00000617027.4:c.508-249G=	ENSP00000483513.1:n.508-249G=
NM_001030047.1:c.*107G=	NP_001025218.1:n.*107G=
NM_001030048.1:c.502-249G=	NP_001025219.1:n.502-249G=
NM_001648.2:c.631-249G= MANE Select	NP_001639.1:n.631-249G=
XM_011526923.1:c.649-249G=	XP_011525225.1:n.649-249G=
XM_011526924.1:c.*107G=	XP_011525226.1:n.*107G=
XR_935817.1:n.1324+469G=