Canonical Allele Identifier: CA407022406

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51361415C>A (hg19) ; chr19:g.50858159C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858159C>A , CM000681.2:g.50858159C>A	GRCh38
NC_000019.9:g.51361415C>A , CM000681.1:g.51361415C>A	GRCh37
NC_000019.8:g.56053227C>A	NCBI36
NG_011653.1:g.8245C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.337C>A MANE Select	ENSP00000314151.1:p.Pro113Thr
ENST00000326003.6:c.337C>A	ENSP00000314151.1:p.Pro113Thr
ENST00000360617.7:c.337C>A	ENSP00000353829.2:p.Pro113Thr
ENST00000422986.6:c.266C>A	ENSP00000393628.2:p.Ala89Asp
ENST00000593997.5:c.337C>A	ENSP00000472907.1:p.Pro113Thr
ENST00000595392.5:c.337C>A	ENSP00000468912.1:p.Pro113Thr
ENST00000595952.5:c.208C>A	ENSP00000471155.1:p.Pro70Thr
ENST00000596185.5:c.*445C>A	ENSP00000471648.1:n.*445C>A
ENST00000596333.1:n.372C>A
ENST00000597286.5:c.226C>A	ENSP00000470523.1:p.Pro76Thr
ENST00000597483.5:c.208C>A	ENSP00000472411.1:p.Pro70Thr
ENST00000598145.1:c.321C>A
ENST00000601349.5:n.1616C>A
ENST00000601503.5:c.280C>A	ENSP00000472213.1:p.Pro94Thr
ENST00000601812.1:n.769C>A
ENST00000617027.4:c.337C>A	ENSP00000483513.1:p.Pro113Thr
NM_001030047.1:c.337C>A	NP_001025218.1:p.Pro113Thr
NM_001030048.1:c.208C>A	NP_001025219.1:p.Pro70Thr
NM_001648.2:c.337C>A MANE Select	NP_001639.1:p.Pro113Thr
XM_011526923.1:c.337C>A	XP_011525225.1:p.Pro113Thr
XM_011526924.1:c.337C>A	XP_011525226.1:p.Pro113Thr
XR_935817.1:n.372C>A