Canonical Allele Identifier: CA2586638925

Gene: KLK3

Linked Data

• gnomAD v4: 19-50859855-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50859855T>G , CM000681.2:g.50859855T>G	GRCh38
NC_000019.9:g.51363111T>G , CM000681.1:g.51363111T>G	GRCh37
NC_000019.8:g.56054923T>G	NCBI36
NG_011653.1:g.9941T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.631-117T>G MANE Select	ENSP00000314151.1:n.631-117T>G
ENST00000326003.6:c.631-117T>G	ENSP00000314151.1:n.631-117T>G
ENST00000360617.7:c.956T>G	ENSP00000353829.2:n.956T>G
ENST00000422986.6:c.*287-117T>G	ENSP00000393628.2:n.*287-117T>G
ENST00000595392.5:c.*132-117T>G	ENSP00000468912.1:n.*132-117T>G
ENST00000595952.5:c.502-117T>G	ENSP00000471155.1:n.502-117T>G
ENST00000596185.5:c.*739-117T>G	ENSP00000471648.1:n.*739-117T>G
ENST00000596333.1:n.809-117T>G
ENST00000598145.1:c.633-117T>G
ENST00000601349.5:n.1910-117T>G
ENST00000601812.1:n.1063-117T>G
ENST00000617027.4:c.508-117T>G	ENSP00000483513.1:n.508-117T>G
NM_001030047.1:c.*239T>G	NP_001025218.1:n.*239T>G
NM_001030048.1:c.502-117T>G	NP_001025219.1:n.502-117T>G
NM_001648.2:c.631-117T>G MANE Select	NP_001639.1:n.631-117T>G
XM_011526923.1:c.649-117T>G	XP_011525225.1:n.649-117T>G
XM_011526924.1:c.*239T>G	XP_011525226.1:n.*239T>G
XR_935817.1:n.1324+601T>G