Canonical Allele Identifier: CA2341115662

Gene: KLK3

Linked Data

• dbSNP Id: rs2090177037
• gnomAD v4: 19-50860236-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860236A>G , CM000681.2:g.50860236A>G	GRCh38
NC_000019.9:g.51363492A>G , CM000681.1:g.51363492A>G	GRCh37
NC_000019.8:g.56055304A>G	NCBI36
NG_011653.1:g.10322A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.*109A>G MANE Select	ENSP00000314151.1:n.*109A>G
ENST00000326003.6:c.*109A>G	ENSP00000314151.1:n.*109A>G
ENST00000360617.7:c.1337A>G	ENSP00000353829.2:n.1337A>G
ENST00000422986.6:c.*551A>G	ENSP00000393628.2:n.*551A>G
ENST00000595392.5:c.*396A>G	ENSP00000468912.1:n.*396A>G
ENST00000595952.5:c.*109A>G	ENSP00000471155.1:n.*109A>G
ENST00000596333.1:n.1073A>G
ENST00000601349.5:n.2174A>G
ENST00000617027.4:c.*109A>G	ENSP00000483513.1:n.*109A>G
NM_001030047.1:c.*620A>G	NP_001025218.1:n.*620A>G
NM_001030048.1:c.*109A>G	NP_001025219.1:n.*109A>G
NM_001648.2:c.*109A>G MANE Select	NP_001639.1:n.*109A>G
XM_011526923.1:c.*109A>G	XP_011525225.1:n.*109A>G
XR_935817.1:n.1324+982A>G