Canonical Allele Identifier: CA407024984

Gene: KLK3

Linked Data

• dbSNP Id: rs1396899450
• gnomAD v2: 19-51363297-T-C
• gnomAD v4: 19-50860041-T-C
• COSMIC: COSM6420939
• MyVariant Identifiers: chr19:g.51363297T>C (hg19) ; chr19:g.50860041T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860041T>C , CM000681.2:g.50860041T>C	GRCh38
NC_000019.9:g.51363297T>C , CM000681.1:g.51363297T>C	GRCh37
NC_000019.8:g.56055109T>C	NCBI36
NG_011653.1:g.10127T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.700T>C MANE Select	ENSP00000314151.1:p.Cys234Arg
ENST00000326003.6:c.700T>C	ENSP00000314151.1:p.Cys234Arg
ENST00000360617.7:c.1142T>C	ENSP00000353829.2:n.1142T>C
ENST00000422986.6:c.*356T>C	ENSP00000393628.2:n.*356T>C
ENST00000595392.5:c.*201T>C	ENSP00000468912.1:n.*201T>C
ENST00000595952.5:c.571T>C	ENSP00000471155.1:p.Cys191Arg
ENST00000596333.1:n.878T>C
ENST00000598145.1:c.702T>C
ENST00000601349.5:n.1979T>C
ENST00000601812.1:n.1132T>C
ENST00000617027.4:c.577T>C	ENSP00000483513.1:p.Cys193Arg
NM_001030047.1:c.*425T>C	NP_001025218.1:n.*425T>C
NM_001030048.1:c.571T>C	NP_001025219.1:p.Cys191Arg
NM_001648.2:c.700T>C MANE Select	NP_001639.1:p.Cys234Arg
XM_011526923.1:c.718T>C	XP_011525225.1:p.Cys240Arg
XR_935817.1:n.1324+787T>C