Canonical Allele Identifier: CA407025002

Gene: KLK3

Linked Data

• dbSNP Id: rs1313860800
• gnomAD v3: 19-50860044-G-A
• gnomAD v4: 19-50860044-G-A
• MyVariant Identifiers: chr19:g.51363300G>A (hg19) ; chr19:g.50860044G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860044G>A , CM000681.2:g.50860044G>A	GRCh38
NC_000019.9:g.51363300G>A , CM000681.1:g.51363300G>A	GRCh37
NC_000019.8:g.56055112G>A	NCBI36
NG_011653.1:g.10130G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.703G>A MANE Select	ENSP00000314151.1:p.Ala235Thr
ENST00000326003.6:c.703G>A	ENSP00000314151.1:p.Ala235Thr
ENST00000360617.7:c.1145G>A	ENSP00000353829.2:n.1145G>A
ENST00000422986.6:c.*359G>A	ENSP00000393628.2:n.*359G>A
ENST00000595392.5:c.*204G>A	ENSP00000468912.1:n.*204G>A
ENST00000595952.5:c.574G>A	ENSP00000471155.1:p.Ala192Thr
ENST00000596333.1:n.881G>A
ENST00000598145.1:c.705G>A
ENST00000601349.5:n.1982G>A
ENST00000601812.1:n.1135G>A
ENST00000617027.4:c.580G>A	ENSP00000483513.1:p.Ala194Thr
NM_001030047.1:c.*428G>A	NP_001025218.1:n.*428G>A
NM_001030048.1:c.574G>A	NP_001025219.1:p.Ala192Thr
NM_001648.2:c.703G>A MANE Select	NP_001639.1:p.Ala235Thr
XM_011526923.1:c.721G>A	XP_011525225.1:p.Ala241Thr
XR_935817.1:n.1324+790G>A