Canonical Allele Identifier: CA407022781

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51361535T>G (hg19) ; chr19:g.50858279T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858279T>G , CM000681.2:g.50858279T>G	GRCh38
NC_000019.9:g.51361535T>G , CM000681.1:g.51361535T>G	GRCh37
NC_000019.8:g.56053347T>G	NCBI36
NG_011653.1:g.8365T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.457T>G MANE Select	ENSP00000314151.1:p.Tyr153Asp
ENST00000326003.6:c.457T>G	ENSP00000314151.1:p.Tyr153Asp
ENST00000360617.7:c.457T>G	ENSP00000353829.2:p.Tyr153Asp
ENST00000422986.6:c.*113T>G	ENSP00000393628.2:n.*113T>G
ENST00000593997.5:c.457T>G	ENSP00000472907.1:p.Tyr153Asp
ENST00000595392.5:c.353-20T>G	ENSP00000468912.1:n.353-20T>G
ENST00000595952.5:c.328T>G	ENSP00000471155.1:p.Tyr110Asp
ENST00000596185.5:c.*565T>G	ENSP00000471648.1:n.*565T>G
ENST00000596333.1:n.492T>G
ENST00000597286.5:c.346T>G	ENSP00000470523.1:p.Tyr116Asp
ENST00000597483.5:c.328T>G	ENSP00000472411.1:p.Tyr110Asp
ENST00000598145.1:c.441T>G
ENST00000601349.5:n.1736T>G
ENST00000601503.5:c.400T>G	ENSP00000472213.1:p.Tyr134Asp
ENST00000601812.1:n.889T>G
ENST00000617027.4:c.354-20T>G	ENSP00000483513.1:n.354-20T>G
NM_001030047.1:c.457T>G	NP_001025218.1:p.Tyr153Asp
NM_001030048.1:c.328T>G	NP_001025219.1:p.Tyr110Asp
NM_001648.2:c.457T>G MANE Select	NP_001639.1:p.Tyr153Asp
XM_011526923.1:c.457T>G	XP_011525225.1:p.Tyr153Asp
XM_011526924.1:c.457T>G	XP_011525226.1:p.Tyr153Asp
XR_935817.1:n.492T>G