Canonical Allele Identifier: CA407022550
Gene: KLK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50858199T>A , CM000681.2:g.50858199T>A GRCh38
NC_000019.9:g.51361455T>A , CM000681.1:g.51361455T>A GRCh37
NC_000019.8:g.56053267T>A NCBI36
NG_011653.1:g.8285T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.377T>A MANE Select ENSP00000314151.1:p.Leu126Gln
ENST00000326003.6:c.377T>A ENSP00000314151.1:p.Leu126Gln
ENST00000360617.7:c.377T>A ENSP00000353829.2:p.Leu126Gln
ENST00000422986.6:c.*33T>A ENSP00000393628.2:n.*33T>A
ENST00000593997.5:c.377T>A ENSP00000472907.1:p.Leu126Gln
ENST00000595392.5:c.352+25T>A ENSP00000468912.1:n.352+25T>A
ENST00000595952.5:c.248T>A ENSP00000471155.1:p.Leu83Gln
ENST00000596185.5:c.*485T>A ENSP00000471648.1:n.*485T>A
ENST00000596333.1:n.412T>A
ENST00000597286.5:c.266T>A ENSP00000470523.1:p.Leu89Gln
ENST00000597483.5:c.248T>A ENSP00000472411.1:p.Leu83Gln
ENST00000598145.1:c.361T>A
ENST00000601349.5:n.1656T>A
ENST00000601503.5:c.320T>A ENSP00000472213.1:p.Leu107Gln
ENST00000601812.1:n.809T>A
ENST00000617027.4:c.353+24T>A ENSP00000483513.1:n.353+24T>A
NM_001030047.1:c.377T>A NP_001025218.1:p.Leu126Gln
NM_001030048.1:c.248T>A NP_001025219.1:p.Leu83Gln
NM_001648.2:c.377T>A MANE Select NP_001639.1:p.Leu126Gln
XM_011526923.1:c.377T>A XP_011525225.1:p.Leu126Gln
XM_011526924.1:c.377T>A XP_011525226.1:p.Leu126Gln
XR_935817.1:n.412T>A