Canonical Allele Identifier: CA407024872

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363255A>T (hg19) ; chr19:g.50859999A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50859999A>T , CM000681.2:g.50859999A>T	GRCh38
NC_000019.9:g.51363255A>T , CM000681.1:g.51363255A>T	GRCh37
NC_000019.8:g.56055067A>T	NCBI36
NG_011653.1:g.10085A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.658A>T MANE Select	ENSP00000314151.1:p.Asn220Tyr
ENST00000326003.6:c.658A>T	ENSP00000314151.1:p.Asn220Tyr
ENST00000360617.7:c.1100A>T	ENSP00000353829.2:n.1100A>T
ENST00000422986.6:c.*314A>T	ENSP00000393628.2:n.*314A>T
ENST00000595392.5:c.*159A>T	ENSP00000468912.1:n.*159A>T
ENST00000595952.5:c.529A>T	ENSP00000471155.1:p.Asn177Tyr
ENST00000596185.5:c.*766A>T	ENSP00000471648.1:n.*766A>T
ENST00000596333.1:n.836A>T
ENST00000598145.1:c.660A>T
ENST00000601349.5:n.1937A>T
ENST00000601812.1:n.1090A>T
ENST00000617027.4:c.535A>T	ENSP00000483513.1:p.Asn179Tyr
NM_001030047.1:c.*383A>T	NP_001025218.1:n.*383A>T
NM_001030048.1:c.529A>T	NP_001025219.1:p.Asn177Tyr
NM_001648.2:c.658A>T MANE Select	NP_001639.1:p.Asn220Tyr
XM_011526923.1:c.676A>T	XP_011525225.1:p.Asn226Tyr
XM_011526924.1:c.*383A>T	XP_011525226.1:n.*383A>T
XR_935817.1:n.1324+745A>T