Canonical Allele Identifier: CA2814740544
Gene: KLK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50859862_50859863insC , CM000681.2:g.50859862_50859863insC GRCh38
NC_000019.9:g.51363118_51363119insC , CM000681.1:g.51363118_51363119insC GRCh37
NC_000019.8:g.56054930_56054931insC NCBI36
NG_011653.1:g.9948_9949insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000326003.7:c.631-110_631-109insC MANE Select ENSP00000314151.1:n.631-110_631-109insC
ENST00000326003.6:c.631-110_631-109insC ENSP00000314151.1:n.631-110_631-109insC
ENST00000360617.7:c.963_964insC ENSP00000353829.2:n.963_964insC
ENST00000422986.6:c.*287-110_*287-109insC ENSP00000393628.2:n.*287-110_*287-109insC
ENST00000595392.5:c.*132-110_*132-109insC ENSP00000468912.1:n.*132-110_*132-109insC
ENST00000595952.5:c.502-110_502-109insC ENSP00000471155.1:n.502-110_502-109insC
ENST00000596185.5:c.*739-110_*739-109insC ENSP00000471648.1:n.*739-110_*739-109insC
ENST00000596333.1:n.809-110_809-109insC
ENST00000598145.1:c.633-110_633-109insC
ENST00000601349.5:n.1910-110_1910-109insC
ENST00000601812.1:n.1063-110_1063-109insC
ENST00000617027.4:c.508-110_508-109insC ENSP00000483513.1:n.508-110_508-109insC
NM_001030047.1:c.*246_*247insC NP_001025218.1:n.*246_*247insC
NM_001030048.1:c.502-110_502-109insC NP_001025219.1:n.502-110_502-109insC
NM_001648.2:c.631-110_631-109insC MANE Select NP_001639.1:n.631-110_631-109insC
XM_011526923.1:c.649-110_649-109insC XP_011525225.1:n.649-110_649-109insC
XM_011526924.1:c.*246_*247insC XP_011525226.1:n.*246_*247insC
XR_935817.1:n.1324+608_1324+609insC