Canonical Allele Identifier: CA508313670

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51361471G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858215G>A , CM000681.2:g.50858215G>A	GRCh38
NC_000019.9:g.51361471G>A , CM000681.1:g.51361471G>A	GRCh37
NC_000019.8:g.56053283G>A	NCBI36
NG_011653.1:g.8301G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.393G>A MANE Select	ENSP00000314151.1:p.Glu131=
ENST00000326003.6:c.393G>A	ENSP00000314151.1:p.Glu131=
ENST00000360617.7:c.393G>A	ENSP00000353829.2:p.Glu131=
ENST00000422986.6:c.*49G>A	ENSP00000393628.2:n.*49G>A
ENST00000593997.5:c.393G>A	ENSP00000472907.1:p.Glu131=
ENST00000595392.5:c.352+41G>A	ENSP00000468912.1:n.352+41G>A
ENST00000595952.5:c.264G>A	ENSP00000471155.1:p.Glu88=
ENST00000596185.5:c.*501G>A	ENSP00000471648.1:n.*501G>A
ENST00000596333.1:n.428G>A
ENST00000597286.5:c.282G>A	ENSP00000470523.1:p.Glu94=
ENST00000597483.5:c.264G>A	ENSP00000472411.1:p.Glu88=
ENST00000598145.1:c.377G>A
ENST00000601349.5:n.1672G>A
ENST00000601503.5:c.336G>A	ENSP00000472213.1:p.Glu112=
ENST00000601812.1:n.825G>A
ENST00000617027.4:c.353+40G>A	ENSP00000483513.1:n.353+40G>A
NM_001030047.1:c.393G>A	NP_001025218.1:p.Glu131=
NM_001030048.1:c.264G>A	NP_001025219.1:p.Glu88=
NM_001648.2:c.393G>A MANE Select	NP_001639.1:p.Glu131=
XM_011526923.1:c.393G>A	XP_011525225.1:p.Glu131=
XM_011526924.1:c.393G>A	XP_011525226.1:p.Glu131=
XR_935817.1:n.428G>A