Canonical Allele Identifier: CA2586639284
Gene: KLK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50860180G>A , CM000681.2:g.50860180G>A GRCh38
NC_000019.9:g.51363436G>A , CM000681.1:g.51363436G>A GRCh37
NC_000019.8:g.56055248G>A NCBI36
NG_011653.1:g.10266G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.*53G>A MANE Select ENSP00000314151.1:n.*53G>A
ENST00000326003.6:c.*53G>A ENSP00000314151.1:n.*53G>A
ENST00000360617.7:c.1281G>A ENSP00000353829.2:n.1281G>A
ENST00000422986.6:c.*495G>A ENSP00000393628.2:n.*495G>A
ENST00000595392.5:c.*340G>A ENSP00000468912.1:n.*340G>A
ENST00000595952.5:c.*53G>A ENSP00000471155.1:n.*53G>A
ENST00000596333.1:n.1017G>A
ENST00000598145.1:c.841G>A
ENST00000601349.5:n.2118G>A
ENST00000617027.4:c.*53G>A ENSP00000483513.1:n.*53G>A
NM_001030047.1:c.*564G>A NP_001025218.1:n.*564G>A
NM_001030048.1:c.*53G>A NP_001025219.1:n.*53G>A
NM_001648.2:c.*53G>A MANE Select NP_001639.1:n.*53G>A
XM_011526923.1:c.*53G>A XP_011525225.1:n.*53G>A
XR_935817.1:n.1324+926G>A