Canonical Allele Identifier: CA407025204

Gene: KLK3

Linked Data

• dbSNP Id: rs1298281756
• gnomAD v2: 19-51363360-G-A
• gnomAD v3: 19-50860104-G-A
• gnomAD v4: 19-50860104-G-A
• MyVariant Identifiers: chr19:g.51363360G>A (hg19) ; chr19:g.50860104G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860104G>A , CM000681.2:g.50860104G>A	GRCh38
NC_000019.9:g.51363360G>A , CM000681.1:g.51363360G>A	GRCh37
NC_000019.8:g.56055172G>A	NCBI36
NG_011653.1:g.10190G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.763G>A MANE Select	ENSP00000314151.1:p.Asp255Asn
ENST00000326003.6:c.763G>A	ENSP00000314151.1:p.Asp255Asn
ENST00000360617.7:c.1205G>A	ENSP00000353829.2:n.1205G>A
ENST00000422986.6:c.*419G>A	ENSP00000393628.2:n.*419G>A
ENST00000595392.5:c.*264G>A	ENSP00000468912.1:n.*264G>A
ENST00000595952.5:c.634G>A	ENSP00000471155.1:p.Asp212Asn
ENST00000596333.1:n.941G>A
ENST00000598145.1:c.765G>A
ENST00000601349.5:n.2042G>A
ENST00000601812.1:n.1195G>A
ENST00000617027.4:c.640G>A	ENSP00000483513.1:p.Asp214Asn
NM_001030047.1:c.*488G>A	NP_001025218.1:n.*488G>A
NM_001030048.1:c.634G>A	NP_001025219.1:p.Asp212Asn
NM_001648.2:c.763G>A MANE Select	NP_001639.1:p.Asp255Asn
XM_011526923.1:c.781G>A	XP_011525225.1:p.Asp261Asn
XR_935817.1:n.1324+850G>A