Canonical Allele Identifier: CA309634156

Gene: KLK3

Linked Data

• dbSNP Id: rs3180906
• gnomAD v4: 19-50860264-C-A
• MyVariant Identifiers: chr19:g.51363520C>A (hg19) ; chr19:g.50860264C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860264C>A , CM000681.2:g.50860264C>A	GRCh38
NC_000019.9:g.51363520C>A , CM000681.1:g.51363520C>A	GRCh37
NC_000019.8:g.56055332C>A	NCBI36
NG_011653.1:g.10350C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.*137C>A MANE Select	ENSP00000314151.1:n.*137C>A
ENST00000326003.6:c.*137C>A	ENSP00000314151.1:n.*137C>A
ENST00000360617.7:c.1365C>A	ENSP00000353829.2:n.1365C>A
ENST00000422986.6:c.*579C>A	ENSP00000393628.2:n.*579C>A
ENST00000595392.5:c.*424C>A	ENSP00000468912.1:n.*424C>A
ENST00000595952.5:c.*137C>A	ENSP00000471155.1:n.*137C>A
ENST00000596333.1:n.1101C>A
ENST00000601349.5:n.2202C>A
ENST00000617027.4:c.*137C>A	ENSP00000483513.1:n.*137C>A
NM_001030047.1:c.*648C>A	NP_001025218.1:n.*648C>A
NM_001030048.1:c.*137C>A	NP_001025219.1:n.*137C>A
NM_001648.2:c.*137C>A MANE Select	NP_001639.1:n.*137C>A
XM_011526923.1:c.*137C>A	XP_011525225.1:n.*137C>A
XR_935817.1:n.1324+1010C>A