Canonical Allele Identifier: CA407025242

Gene: KLK3

Linked Data

• dbSNP Id: rs2090175807
• gnomAD v3: 19-50860116-G-A
• gnomAD v4: 19-50860116-G-A
• MyVariant Identifiers: chr19:g.51363372G>A (hg19) ; chr19:g.50860116G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860116G>A , CM000681.2:g.50860116G>A	GRCh38
NC_000019.9:g.51363372G>A , CM000681.1:g.51363372G>A	GRCh37
NC_000019.8:g.56055184G>A	NCBI36
NG_011653.1:g.10202G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.775G>A MANE Select	ENSP00000314151.1:p.Ala259Thr
ENST00000326003.6:c.775G>A	ENSP00000314151.1:p.Ala259Thr
ENST00000360617.7:c.1217G>A	ENSP00000353829.2:n.1217G>A
ENST00000422986.6:c.*431G>A	ENSP00000393628.2:n.*431G>A
ENST00000595392.5:c.*276G>A	ENSP00000468912.1:n.*276G>A
ENST00000595952.5:c.646G>A	ENSP00000471155.1:p.Ala216Thr
ENST00000596333.1:n.953G>A
ENST00000598145.1:c.777G>A
ENST00000601349.5:n.2054G>A
ENST00000601812.1:n.1207G>A
ENST00000617027.4:c.652G>A	ENSP00000483513.1:p.Ala218Thr
NM_001030047.1:c.*500G>A	NP_001025218.1:n.*500G>A
NM_001030048.1:c.646G>A	NP_001025219.1:p.Ala216Thr
NM_001648.2:c.775G>A MANE Select	NP_001639.1:p.Ala259Thr
XM_011526923.1:c.793G>A	XP_011525225.1:p.Ala265Thr
XR_935817.1:n.1324+862G>A