Canonical Allele Identifier: CA2586638906

Gene: KLK3

Linked Data

• gnomAD v4: 19-50859819-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50859819C>A , CM000681.2:g.50859819C>A	GRCh38
NC_000019.9:g.51363075C>A , CM000681.1:g.51363075C>A	GRCh37
NC_000019.8:g.56054887C>A	NCBI36
NG_011653.1:g.9905C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.631-153C>A MANE Select	ENSP00000314151.1:n.631-153C>A
ENST00000326003.6:c.631-153C>A	ENSP00000314151.1:n.631-153C>A
ENST00000360617.7:c.920C>A	ENSP00000353829.2:n.920C>A
ENST00000422986.6:c.*287-153C>A	ENSP00000393628.2:n.*287-153C>A
ENST00000595392.5:c.*132-153C>A	ENSP00000468912.1:n.*132-153C>A
ENST00000595952.5:c.502-153C>A	ENSP00000471155.1:n.502-153C>A
ENST00000596185.5:c.*739-153C>A	ENSP00000471648.1:n.*739-153C>A
ENST00000596333.1:n.809-153C>A
ENST00000598145.1:c.633-153C>A
ENST00000601349.5:n.1910-153C>A
ENST00000601812.1:n.1063-153C>A
ENST00000617027.4:c.508-153C>A	ENSP00000483513.1:n.508-153C>A
NM_001030047.1:c.*203C>A	NP_001025218.1:n.*203C>A
NM_001030048.1:c.502-153C>A	NP_001025219.1:n.502-153C>A
NM_001648.2:c.631-153C>A MANE Select	NP_001639.1:n.631-153C>A
XM_011526923.1:c.649-153C>A	XP_011525225.1:n.649-153C>A
XM_011526924.1:c.*203C>A	XP_011525226.1:n.*203C>A
XR_935817.1:n.1324+565C>A