Canonical Allele Identifier: CA2341114629

Gene: KLK3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858306C= , CM000681.2:g.50858306C=	GRCh38
NC_000019.9:g.51361562C= , CM000681.1:g.51361562C=	GRCh37
NC_000019.8:g.56053374C=	NCBI36
NG_011653.1:g.8392C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.484C= MANE Select	ENSP00000314151.1:p.Pro162=
ENST00000326003.6:c.484C=	ENSP00000314151.1:p.Pro162=
ENST00000360617.7:c.484C=	ENSP00000353829.2:p.Pro162=
ENST00000422986.6:c.*140C=	ENSP00000393628.2:n.*140C=
ENST00000593997.5:c.484C=	ENSP00000472907.1:p.Pro162=
ENST00000595392.5:c.360C=	ENSP00000468912.1:p.Asn120=
ENST00000595952.5:c.355C=	ENSP00000471155.1:p.Pro119=
ENST00000596185.5:c.*592C=	ENSP00000471648.1:n.*592C=
ENST00000596333.1:n.519C=
ENST00000597286.5:c.373C=	ENSP00000470523.1:p.Pro125=
ENST00000597483.5:c.355C=	ENSP00000472411.1:p.Pro119=
ENST00000598145.1:c.468C=
ENST00000601349.5:n.1763C=
ENST00000601503.5:c.427C=	ENSP00000472213.1:p.Pro143=
ENST00000601812.1:n.916C=
ENST00000617027.4:c.361C=	ENSP00000483513.1:p.Pro121=
NM_001030047.1:c.484C=	NP_001025218.1:p.Pro162=
NM_001030048.1:c.355C=	NP_001025219.1:p.Pro119=
NM_001648.2:c.484C= MANE Select	NP_001639.1:p.Pro162=
XM_011526923.1:c.484C=	XP_011525225.1:p.Pro162=
XM_011526924.1:c.484C=	XP_011525226.1:p.Pro162=
XR_935817.1:n.519C=