Canonical Allele Identifier: CA407025161

Gene: KLK3

Linked Data

• gnomAD v4: 19-50860084-A-G
• MyVariant Identifiers: chr19:g.51363340A>G (hg19) ; chr19:g.50860084A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860084A>G , CM000681.2:g.50860084A>G	GRCh38
NC_000019.9:g.51363340A>G , CM000681.1:g.51363340A>G	GRCh37
NC_000019.8:g.56055152A>G	NCBI36
NG_011653.1:g.10170A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.743A>G MANE Select	ENSP00000314151.1:p.His248Arg
ENST00000326003.6:c.743A>G	ENSP00000314151.1:p.His248Arg
ENST00000360617.7:c.1185A>G	ENSP00000353829.2:n.1185A>G
ENST00000422986.6:c.*399A>G	ENSP00000393628.2:n.*399A>G
ENST00000595392.5:c.*244A>G	ENSP00000468912.1:n.*244A>G
ENST00000595952.5:c.614A>G	ENSP00000471155.1:p.His205Arg
ENST00000596333.1:n.921A>G
ENST00000598145.1:c.745A>G
ENST00000601349.5:n.2022A>G
ENST00000601812.1:n.1175A>G
ENST00000617027.4:c.620A>G	ENSP00000483513.1:p.His207Arg
NM_001030047.1:c.*468A>G	NP_001025218.1:n.*468A>G
NM_001030048.1:c.614A>G	NP_001025219.1:p.His205Arg
NM_001648.2:c.743A>G MANE Select	NP_001639.1:p.His248Arg
XM_011526923.1:c.761A>G	XP_011525225.1:p.His254Arg
XR_935817.1:n.1324+830A>G