Canonical Allele Identifier: CA407025205

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363360G>C (hg19) ; chr19:g.50860104G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860104G>C , CM000681.2:g.50860104G>C	GRCh38
NC_000019.9:g.51363360G>C , CM000681.1:g.51363360G>C	GRCh37
NC_000019.8:g.56055172G>C	NCBI36
NG_011653.1:g.10190G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.763G>C MANE Select	ENSP00000314151.1:p.Asp255His
ENST00000326003.6:c.763G>C	ENSP00000314151.1:p.Asp255His
ENST00000360617.7:c.1205G>C	ENSP00000353829.2:n.1205G>C
ENST00000422986.6:c.*419G>C	ENSP00000393628.2:n.*419G>C
ENST00000595392.5:c.*264G>C	ENSP00000468912.1:n.*264G>C
ENST00000595952.5:c.634G>C	ENSP00000471155.1:p.Asp212His
ENST00000596333.1:n.941G>C
ENST00000598145.1:c.765G>C
ENST00000601349.5:n.2042G>C
ENST00000601812.1:n.1195G>C
ENST00000617027.4:c.640G>C	ENSP00000483513.1:p.Asp214His
NM_001030047.1:c.*488G>C	NP_001025218.1:n.*488G>C
NM_001030048.1:c.634G>C	NP_001025219.1:p.Asp212His
NM_001648.2:c.763G>C MANE Select	NP_001639.1:p.Asp255His
XM_011526923.1:c.781G>C	XP_011525225.1:p.Asp261His
XR_935817.1:n.1324+850G>C