Canonical Allele Identifier: CA407024928

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363282T>C (hg19) ; chr19:g.50860026T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860026T>C , CM000681.2:g.50860026T>C	GRCh38
NC_000019.9:g.51363282T>C , CM000681.1:g.51363282T>C	GRCh37
NC_000019.8:g.56055094T>C	NCBI36
NG_011653.1:g.10112T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.685T>C MANE Select	ENSP00000314151.1:p.Trp229Arg
ENST00000326003.6:c.685T>C	ENSP00000314151.1:p.Trp229Arg
ENST00000360617.7:c.1127T>C	ENSP00000353829.2:n.1127T>C
ENST00000422986.6:c.*341T>C	ENSP00000393628.2:n.*341T>C
ENST00000595392.5:c.*186T>C	ENSP00000468912.1:n.*186T>C
ENST00000595952.5:c.556T>C	ENSP00000471155.1:p.Trp186Arg
ENST00000596333.1:n.863T>C
ENST00000598145.1:c.687T>C
ENST00000601349.5:n.1964T>C
ENST00000601812.1:n.1117T>C
ENST00000617027.4:c.562T>C	ENSP00000483513.1:p.Trp188Arg
NM_001030047.1:c.*410T>C	NP_001025218.1:n.*410T>C
NM_001030048.1:c.556T>C	NP_001025219.1:p.Trp186Arg
NM_001648.2:c.685T>C MANE Select	NP_001639.1:p.Trp229Arg
XM_011526923.1:c.703T>C	XP_011525225.1:p.Trp235Arg
XR_935817.1:n.1324+772T>C