Canonical Allele Identifier: CA407024873

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363256A>C (hg19) ; chr19:g.50860000A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860000A>C , CM000681.2:g.50860000A>C	GRCh38
NC_000019.9:g.51363256A>C , CM000681.1:g.51363256A>C	GRCh37
NC_000019.8:g.56055068A>C	NCBI36
NG_011653.1:g.10086A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.659A>C MANE Select	ENSP00000314151.1:p.Asn220Thr
ENST00000326003.6:c.659A>C	ENSP00000314151.1:p.Asn220Thr
ENST00000360617.7:c.1101A>C	ENSP00000353829.2:n.1101A>C
ENST00000422986.6:c.*315A>C	ENSP00000393628.2:n.*315A>C
ENST00000595392.5:c.*160A>C	ENSP00000468912.1:n.*160A>C
ENST00000595952.5:c.530A>C	ENSP00000471155.1:p.Asn177Thr
ENST00000596185.5:c.*767A>C	ENSP00000471648.1:n.*767A>C
ENST00000596333.1:n.837A>C
ENST00000598145.1:c.661A>C
ENST00000601349.5:n.1938A>C
ENST00000601812.1:n.1091A>C
ENST00000617027.4:c.536A>C	ENSP00000483513.1:p.Asn179Thr
NM_001030047.1:c.*384A>C	NP_001025218.1:n.*384A>C
NM_001030048.1:c.530A>C	NP_001025219.1:p.Asn177Thr
NM_001648.2:c.659A>C MANE Select	NP_001639.1:p.Asn220Thr
XM_011526923.1:c.677A>C	XP_011525225.1:p.Asn226Thr
XM_011526924.1:c.*384A>C	XP_011525226.1:n.*384A>C
XR_935817.1:n.1324+746A>C