Canonical Allele Identifier: CA407022442
Gene: KLK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50858170C>G , CM000681.2:g.50858170C>G GRCh38
NC_000019.9:g.51361426C>G , CM000681.1:g.51361426C>G GRCh37
NC_000019.8:g.56053238C>G NCBI36
NG_011653.1:g.8256C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.348C>G MANE Select ENSP00000314151.1:p.Asp116Glu
ENST00000326003.6:c.348C>G ENSP00000314151.1:p.Asp116Glu
ENST00000360617.7:c.348C>G ENSP00000353829.2:p.Asp116Glu
ENST00000422986.6:c.*4C>G ENSP00000393628.2:n.*4C>G
ENST00000593997.5:c.348C>G ENSP00000472907.1:p.Asp116Glu
ENST00000595392.5:c.348C>G ENSP00000468912.1:p.Asp116Glu
ENST00000595952.5:c.219C>G ENSP00000471155.1:p.Asp73Glu
ENST00000596185.5:c.*456C>G ENSP00000471648.1:n.*456C>G
ENST00000596333.1:n.383C>G
ENST00000597286.5:c.237C>G ENSP00000470523.1:p.Asp79Glu
ENST00000597483.5:c.219C>G ENSP00000472411.1:p.Asp73Glu
ENST00000598145.1:c.332C>G
ENST00000601349.5:n.1627C>G
ENST00000601503.5:c.291C>G ENSP00000472213.1:p.Asp97Glu
ENST00000601812.1:n.780C>G
ENST00000617027.4:c.348C>G ENSP00000483513.1:p.Asp116Glu
NM_001030047.1:c.348C>G NP_001025218.1:p.Asp116Glu
NM_001030048.1:c.219C>G NP_001025219.1:p.Asp73Glu
NM_001648.2:c.348C>G MANE Select NP_001639.1:p.Asp116Glu
XM_011526923.1:c.348C>G XP_011525225.1:p.Asp116Glu
XM_011526924.1:c.348C>G XP_011525226.1:p.Asp116Glu
XR_935817.1:n.383C>G