Canonical Allele Identifier: CA407025166

Gene: KLK3

Linked Data

• gnomAD v4: 19-50860087-A-G
• MyVariant Identifiers: chr19:g.51363343A>G (hg19) ; chr19:g.50860087A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860087A>G , CM000681.2:g.50860087A>G	GRCh38
NC_000019.9:g.51363343A>G , CM000681.1:g.51363343A>G	GRCh37
NC_000019.8:g.56055155A>G	NCBI36
NG_011653.1:g.10173A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.746A>G MANE Select	ENSP00000314151.1:p.Tyr249Cys
ENST00000326003.6:c.746A>G	ENSP00000314151.1:p.Tyr249Cys
ENST00000360617.7:c.1188A>G	ENSP00000353829.2:n.1188A>G
ENST00000422986.6:c.*402A>G	ENSP00000393628.2:n.*402A>G
ENST00000595392.5:c.*247A>G	ENSP00000468912.1:n.*247A>G
ENST00000595952.5:c.617A>G	ENSP00000471155.1:p.Tyr206Cys
ENST00000596333.1:n.924A>G
ENST00000598145.1:c.748A>G
ENST00000601349.5:n.2025A>G
ENST00000601812.1:n.1178A>G
ENST00000617027.4:c.623A>G	ENSP00000483513.1:p.Tyr208Cys
NM_001030047.1:c.*471A>G	NP_001025218.1:n.*471A>G
NM_001030048.1:c.617A>G	NP_001025219.1:p.Tyr206Cys
NM_001648.2:c.746A>G MANE Select	NP_001639.1:p.Tyr249Cys
XM_011526923.1:c.764A>G	XP_011525225.1:p.Tyr255Cys
XR_935817.1:n.1324+833A>G