Canonical Allele Identifier: CA9604613

Gene: KLK3

Linked Data

• dbSNP Id: rs780743219
• ExAC: 19:51363378 C / A
• gnomAD v2: 19-51363378-C-A
• gnomAD v4: 19-50860122-C-A
• MyVariant Identifiers: chr19:g.51363378C>A (hg19) ; chr19:g.50860122C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860122C>A , CM000681.2:g.50860122C>A	GRCh38
NC_000019.9:g.51363378C>A , CM000681.1:g.51363378C>A	GRCh37
NC_000019.8:g.56055190C>A	NCBI36
NG_011653.1:g.10208C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.781C>A MANE Select	ENSP00000314151.1:p.Pro261Thr
ENST00000326003.6:c.781C>A	ENSP00000314151.1:p.Pro261Thr
ENST00000360617.7:c.1223C>A	ENSP00000353829.2:n.1223C>A
ENST00000422986.6:c.*437C>A	ENSP00000393628.2:n.*437C>A
ENST00000595392.5:c.*282C>A	ENSP00000468912.1:n.*282C>A
ENST00000595952.5:c.652C>A	ENSP00000471155.1:p.Pro218Thr
ENST00000596333.1:n.959C>A
ENST00000598145.1:c.783C>A
ENST00000601349.5:n.2060C>A
ENST00000601812.1:n.1213C>A
ENST00000617027.4:c.658C>A	ENSP00000483513.1:p.Pro220Thr
NM_001030047.1:c.*506C>A	NP_001025218.1:n.*506C>A
NM_001030048.1:c.652C>A	NP_001025219.1:p.Pro218Thr
NM_001648.2:c.781C>A MANE Select	NP_001639.1:p.Pro261Thr
XM_011526923.1:c.799C>A	XP_011525225.1:p.Pro267Thr
XR_935817.1:n.1324+868C>A