Canonical Allele Identifier: CA407025256

Gene: KLK3

Linked Data

• COSMIC: COSM4793123
• MyVariant Identifiers: chr19:g.51363375A>T (hg19) ; chr19:g.50860119A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860119A>T , CM000681.2:g.50860119A>T	GRCh38
NC_000019.9:g.51363375A>T , CM000681.1:g.51363375A>T	GRCh37
NC_000019.8:g.56055187A>T	NCBI36
NG_011653.1:g.10205A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.778A>T MANE Select	ENSP00000314151.1:p.Asn260Tyr
ENST00000326003.6:c.778A>T	ENSP00000314151.1:p.Asn260Tyr
ENST00000360617.7:c.1220A>T	ENSP00000353829.2:n.1220A>T
ENST00000422986.6:c.*434A>T	ENSP00000393628.2:n.*434A>T
ENST00000595392.5:c.*279A>T	ENSP00000468912.1:n.*279A>T
ENST00000595952.5:c.649A>T	ENSP00000471155.1:p.Asn217Tyr
ENST00000596333.1:n.956A>T
ENST00000598145.1:c.780A>T
ENST00000601349.5:n.2057A>T
ENST00000601812.1:n.1210A>T
ENST00000617027.4:c.655A>T	ENSP00000483513.1:p.Asn219Tyr
NM_001030047.1:c.*503A>T	NP_001025218.1:n.*503A>T
NM_001030048.1:c.649A>T	NP_001025219.1:p.Asn217Tyr
NM_001648.2:c.778A>T MANE Select	NP_001639.1:p.Asn260Tyr
XM_011526923.1:c.796A>T	XP_011525225.1:p.Asn266Tyr
XR_935817.1:n.1324+865A>T