Canonical Allele Identifier: CA2586636965
Gene: KLK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50856849C>A , CM000681.2:g.50856849C>A GRCh38
NC_000019.9:g.51360105C>A , CM000681.1:g.51360105C>A GRCh37
NC_000019.8:g.56051917C>A NCBI36
NG_011653.1:g.6935C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000326003.7:c.206+450C>A MANE Select ENSP00000314151.1:n.206+450C>A
ENST00000326003.6:c.206+450C>A ENSP00000314151.1:n.206+450C>A
ENST00000360617.7:c.206+450C>A ENSP00000353829.2:n.206+450C>A
ENST00000422986.6:c.206+450C>A ENSP00000393628.2:n.206+450C>A
ENST00000593997.5:c.206+450C>A ENSP00000472907.1:n.206+450C>A
ENST00000595392.5:c.206+450C>A ENSP00000468912.1:n.206+450C>A
ENST00000595952.5:c.206+450C>A ENSP00000471155.1:n.206+450C>A
ENST00000596185.5:c.*314+450C>A ENSP00000471648.1:n.*314+450C>A
ENST00000596333.1:n.241+450C>A
ENST00000597286.5:c.95+450C>A ENSP00000470523.1:n.95+450C>A
ENST00000597483.5:c.206+450C>A ENSP00000472411.1:n.206+450C>A
ENST00000598145.1:c.190+450C>A
ENST00000601349.5:n.1485+450C>A
ENST00000601503.5:c.149+450C>A ENSP00000472213.1:n.149+450C>A
ENST00000617027.4:c.206+450C>A ENSP00000483513.1:n.206+450C>A
NM_001030047.1:c.206+450C>A NP_001025218.1:n.206+450C>A
NM_001030048.1:c.206+450C>A NP_001025219.1:n.206+450C>A
NM_001648.2:c.206+450C>A MANE Select NP_001639.1:n.206+450C>A
XM_011526923.1:c.206+450C>A XP_011525225.1:n.206+450C>A
XM_011526924.1:c.206+450C>A XP_011525226.1:n.206+450C>A
XR_935817.1:n.241+450C>A