Canonical Allele Identifier: CA508313698

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51361516A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858260A>C , CM000681.2:g.50858260A>C	GRCh38
NC_000019.9:g.51361516A>C , CM000681.1:g.51361516A>C	GRCh37
NC_000019.8:g.56053328A>C	NCBI36
NG_011653.1:g.8346A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.438A>C MANE Select	ENSP00000314151.1:p.Pro146=
ENST00000326003.6:c.438A>C	ENSP00000314151.1:p.Pro146=
ENST00000360617.7:c.438A>C	ENSP00000353829.2:p.Pro146=
ENST00000422986.6:c.*94A>C	ENSP00000393628.2:n.*94A>C
ENST00000593997.5:c.438A>C	ENSP00000472907.1:p.Pro146=
ENST00000595392.5:c.353-39A>C	ENSP00000468912.1:n.353-39A>C
ENST00000595952.5:c.309A>C	ENSP00000471155.1:p.Pro103=
ENST00000596185.5:c.*546A>C	ENSP00000471648.1:n.*546A>C
ENST00000596333.1:n.473A>C
ENST00000597286.5:c.327A>C	ENSP00000470523.1:p.Pro109=
ENST00000597483.5:c.309A>C	ENSP00000472411.1:p.Pro103=
ENST00000598145.1:c.422A>C
ENST00000601349.5:n.1717A>C
ENST00000601503.5:c.381A>C	ENSP00000472213.1:p.Pro127=
ENST00000601812.1:n.870A>C
ENST00000617027.4:c.354-39A>C	ENSP00000483513.1:n.354-39A>C
NM_001030047.1:c.438A>C	NP_001025218.1:p.Pro146=
NM_001030048.1:c.309A>C	NP_001025219.1:p.Pro103=
NM_001648.2:c.438A>C MANE Select	NP_001639.1:p.Pro146=
XM_011526923.1:c.438A>C	XP_011525225.1:p.Pro146=
XM_011526924.1:c.438A>C	XP_011525226.1:p.Pro146=
XR_935817.1:n.473A>C