Canonical Allele Identifier: CA2341114602

Gene: KLK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858230G= , CM000681.2:g.50858230G=	GRCh38
NC_000019.9:g.51361486G= , CM000681.1:g.51361486G=	GRCh37
NC_000019.8:g.56053298G=	NCBI36
NG_011653.1:g.8316G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.408G= MANE Select	ENSP00000314151.1:p.Val136=
ENST00000326003.6:c.408G=	ENSP00000314151.1:p.Val136=
ENST00000360617.7:c.408G=	ENSP00000353829.2:p.Val136=
ENST00000422986.6:c.*64G=	ENSP00000393628.2:n.*64G=
ENST00000593997.5:c.408G=	ENSP00000472907.1:p.Val136=
ENST00000595392.5:c.352+56G=	ENSP00000468912.1:n.352+56G=
ENST00000595952.5:c.279G=	ENSP00000471155.1:p.Val93=
ENST00000596185.5:c.*516G=	ENSP00000471648.1:n.*516G=
ENST00000596333.1:n.443G=
ENST00000597286.5:c.297G=	ENSP00000470523.1:p.Val99=
ENST00000597483.5:c.279G=	ENSP00000472411.1:p.Val93=
ENST00000598145.1:c.392G=
ENST00000601349.5:n.1687G=
ENST00000601503.5:c.351G=	ENSP00000472213.1:p.Val117=
ENST00000601812.1:n.840G=
ENST00000617027.4:c.353+55G=	ENSP00000483513.1:n.353+55G=
NM_001030047.1:c.408G=	NP_001025218.1:p.Val136=
NM_001030048.1:c.279G=	NP_001025219.1:p.Val93=
NM_001648.2:c.408G= MANE Select	NP_001639.1:p.Val136=
XM_011526923.1:c.408G=	XP_011525225.1:p.Val136=
XM_011526924.1:c.408G=	XP_011525226.1:p.Val136=
XR_935817.1:n.443G=