Canonical Allele Identifier: CA407025139

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363331A>C (hg19) ; chr19:g.50860075A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860075A>C , CM000681.2:g.50860075A>C	GRCh38
NC_000019.9:g.51363331A>C , CM000681.1:g.51363331A>C	GRCh37
NC_000019.8:g.56055143A>C	NCBI36
NG_011653.1:g.10161A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.734A>C MANE Select	ENSP00000314151.1:p.Lys245Thr
ENST00000326003.6:c.734A>C	ENSP00000314151.1:p.Lys245Thr
ENST00000360617.7:c.1176A>C	ENSP00000353829.2:n.1176A>C
ENST00000422986.6:c.*390A>C	ENSP00000393628.2:n.*390A>C
ENST00000595392.5:c.*235A>C	ENSP00000468912.1:n.*235A>C
ENST00000595952.5:c.605A>C	ENSP00000471155.1:p.Lys202Thr
ENST00000596333.1:n.912A>C
ENST00000598145.1:c.736A>C
ENST00000601349.5:n.2013A>C
ENST00000601812.1:n.1166A>C
ENST00000617027.4:c.611A>C	ENSP00000483513.1:p.Lys204Thr
NM_001030047.1:c.*459A>C	NP_001025218.1:n.*459A>C
NM_001030048.1:c.605A>C	NP_001025219.1:p.Lys202Thr
NM_001648.2:c.734A>C MANE Select	NP_001639.1:p.Lys245Thr
XM_011526923.1:c.752A>C	XP_011525225.1:p.Lys251Thr
XR_935817.1:n.1324+821A>C