Canonical Allele Identifier: CA883222101

Gene: KLK3

Linked Data

• dbSNP Id: rs1185780429
• gnomAD v4: 19-50860198-C-A
• MyVariant Identifiers: chr19:g.51363454C>A (hg19) ; chr19:g.50860198C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860198C>A , CM000681.2:g.50860198C>A	GRCh38
NC_000019.9:g.51363454C>A , CM000681.1:g.51363454C>A	GRCh37
NC_000019.8:g.56055266C>A	NCBI36
NG_011653.1:g.10284C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.*71C>A MANE Select	ENSP00000314151.1:n.*71C>A
ENST00000326003.6:c.*71C>A	ENSP00000314151.1:n.*71C>A
ENST00000360617.7:c.1299C>A	ENSP00000353829.2:n.1299C>A
ENST00000422986.6:c.*513C>A	ENSP00000393628.2:n.*513C>A
ENST00000595392.5:c.*358C>A	ENSP00000468912.1:n.*358C>A
ENST00000595952.5:c.*71C>A	ENSP00000471155.1:n.*71C>A
ENST00000596333.1:n.1035C>A
ENST00000598145.1:c.859C>A
ENST00000601349.5:n.2136C>A
ENST00000617027.4:c.*71C>A	ENSP00000483513.1:n.*71C>A
NM_001030047.1:c.*582C>A	NP_001025218.1:n.*582C>A
NM_001030048.1:c.*71C>A	NP_001025219.1:n.*71C>A
NM_001648.2:c.*71C>A MANE Select	NP_001639.1:n.*71C>A
XM_011526923.1:c.*71C>A	XP_011525225.1:n.*71C>A
XR_935817.1:n.1324+944C>A