Canonical Allele Identifier: CA9604597

Gene: KLK3

Linked Data

• dbSNP Id: rs144118163
• ExAC: 19:51363306 C / A
• gnomAD v2: 19-51363306-C-A
• gnomAD v3: 19-50860050-C-A
• gnomAD v4: 19-50860050-C-A
• MyVariant Identifiers: chr19:g.51363306C>A (hg19) ; chr19:g.50860050C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860050C>A , CM000681.2:g.50860050C>A	GRCh38
NC_000019.9:g.51363306C>A , CM000681.1:g.51363306C>A	GRCh37
NC_000019.8:g.56055118C>A	NCBI36
NG_011653.1:g.10136C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.709C>A MANE Select	ENSP00000314151.1:p.Pro237Thr
ENST00000326003.6:c.709C>A	ENSP00000314151.1:p.Pro237Thr
ENST00000360617.7:c.1151C>A	ENSP00000353829.2:n.1151C>A
ENST00000422986.6:c.*365C>A	ENSP00000393628.2:n.*365C>A
ENST00000595392.5:c.*210C>A	ENSP00000468912.1:n.*210C>A
ENST00000595952.5:c.580C>A	ENSP00000471155.1:p.Pro194Thr
ENST00000596333.1:n.887C>A
ENST00000598145.1:c.711C>A
ENST00000601349.5:n.1988C>A
ENST00000601812.1:n.1141C>A
ENST00000617027.4:c.586C>A	ENSP00000483513.1:p.Pro196Thr
NM_001030047.1:c.*434C>A	NP_001025218.1:n.*434C>A
NM_001030048.1:c.580C>A	NP_001025219.1:p.Pro194Thr
NM_001648.2:c.709C>A MANE Select	NP_001639.1:p.Pro237Thr
XM_011526923.1:c.727C>A	XP_011525225.1:p.Pro243Thr
XR_935817.1:n.1324+796C>A