Canonical Allele Identifier: CA9604581

Gene: KLK3

Linked Data

• dbSNP Id: rs764431782
• ExAC: 19:51363211 C / A
• gnomAD v2: 19-51363211-C-A
• gnomAD v4: 19-50859955-C-A
• MyVariant Identifiers: chr19:g.51363211C>A (hg19) ; chr19:g.50859955C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50859955C>A , CM000681.2:g.50859955C>A	GRCh38
NC_000019.9:g.51363211C>A , CM000681.1:g.51363211C>A	GRCh37
NC_000019.8:g.56055023C>A	NCBI36
NG_011653.1:g.10041C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.631-17C>A MANE Select	ENSP00000314151.1:n.631-17C>A
ENST00000326003.6:c.631-17C>A	ENSP00000314151.1:n.631-17C>A
ENST00000360617.7:c.1056C>A	ENSP00000353829.2:n.1056C>A
ENST00000422986.6:c.*287-17C>A	ENSP00000393628.2:n.*287-17C>A
ENST00000595392.5:c.*132-17C>A	ENSP00000468912.1:n.*132-17C>A
ENST00000595952.5:c.502-17C>A	ENSP00000471155.1:n.502-17C>A
ENST00000596185.5:c.*739-17C>A	ENSP00000471648.1:n.*739-17C>A
ENST00000596333.1:n.809-17C>A
ENST00000598145.1:c.633-17C>A
ENST00000601349.5:n.1910-17C>A
ENST00000601812.1:n.1063-17C>A
ENST00000617027.4:c.508-17C>A	ENSP00000483513.1:n.508-17C>A
NM_001030047.1:c.*339C>A	NP_001025218.1:n.*339C>A
NM_001030048.1:c.502-17C>A	NP_001025219.1:n.502-17C>A
NM_001648.2:c.631-17C>A MANE Select	NP_001639.1:n.631-17C>A
XM_011526923.1:c.649-17C>A	XP_011525225.1:n.649-17C>A
XM_011526924.1:c.*339C>A	XP_011525226.1:n.*339C>A
XR_935817.1:n.1324+701C>A