Canonical Allele Identifier: CA2586638887
Gene: KLK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50859801G>T , CM000681.2:g.50859801G>T GRCh38
NC_000019.9:g.51363057G>T , CM000681.1:g.51363057G>T GRCh37
NC_000019.8:g.56054869G>T NCBI36
NG_011653.1:g.9887G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.631-171G>T MANE Select ENSP00000314151.1:n.631-171G>T
ENST00000326003.6:c.631-171G>T ENSP00000314151.1:n.631-171G>T
ENST00000360617.7:c.902G>T ENSP00000353829.2:n.902G>T
ENST00000422986.6:c.*287-171G>T ENSP00000393628.2:n.*287-171G>T
ENST00000595392.5:c.*132-171G>T ENSP00000468912.1:n.*132-171G>T
ENST00000595952.5:c.502-171G>T ENSP00000471155.1:n.502-171G>T
ENST00000596185.5:c.*739-171G>T ENSP00000471648.1:n.*739-171G>T
ENST00000596333.1:n.809-171G>T
ENST00000597483.5:c.*185G>T ENSP00000472411.1:n.*185G>T
ENST00000598145.1:c.633-171G>T
ENST00000601349.5:n.1910-171G>T
ENST00000601812.1:n.1063-171G>T
ENST00000617027.4:c.508-171G>T ENSP00000483513.1:n.508-171G>T
NM_001030047.1:c.*185G>T NP_001025218.1:n.*185G>T
NM_001030048.1:c.502-171G>T NP_001025219.1:n.502-171G>T
NM_001648.2:c.631-171G>T MANE Select NP_001639.1:n.631-171G>T
XM_011526923.1:c.649-171G>T XP_011525225.1:n.649-171G>T
XM_011526924.1:c.*185G>T XP_011525226.1:n.*185G>T
XR_935817.1:n.1324+547G>T