Canonical Allele Identifier: CA407025159

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363339C>T (hg19) ; chr19:g.50860083C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860083C>T , CM000681.2:g.50860083C>T	GRCh38
NC_000019.9:g.51363339C>T , CM000681.1:g.51363339C>T	GRCh37
NC_000019.8:g.56055151C>T	NCBI36
NG_011653.1:g.10169C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.742C>T MANE Select	ENSP00000314151.1:p.His248Tyr
ENST00000326003.6:c.742C>T	ENSP00000314151.1:p.His248Tyr
ENST00000360617.7:c.1184C>T	ENSP00000353829.2:n.1184C>T
ENST00000422986.6:c.*398C>T	ENSP00000393628.2:n.*398C>T
ENST00000595392.5:c.*243C>T	ENSP00000468912.1:n.*243C>T
ENST00000595952.5:c.613C>T	ENSP00000471155.1:p.His205Tyr
ENST00000596333.1:n.920C>T
ENST00000598145.1:c.744C>T
ENST00000601349.5:n.2021C>T
ENST00000601812.1:n.1174C>T
ENST00000617027.4:c.619C>T	ENSP00000483513.1:p.His207Tyr
NM_001030047.1:c.*467C>T	NP_001025218.1:n.*467C>T
NM_001030048.1:c.613C>T	NP_001025219.1:p.His205Tyr
NM_001648.2:c.742C>T MANE Select	NP_001639.1:p.His248Tyr
XM_011526923.1:c.760C>T	XP_011525225.1:p.His254Tyr
XR_935817.1:n.1324+829C>T