Canonical Allele Identifier: CA407025103

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363324T>C (hg19) ; chr19:g.50860068T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860068T>C , CM000681.2:g.50860068T>C	GRCh38
NC_000019.9:g.51363324T>C , CM000681.1:g.51363324T>C	GRCh37
NC_000019.8:g.56055136T>C	NCBI36
NG_011653.1:g.10154T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.727T>C MANE Select	ENSP00000314151.1:p.Tyr243His
ENST00000326003.6:c.727T>C	ENSP00000314151.1:p.Tyr243His
ENST00000360617.7:c.1169T>C	ENSP00000353829.2:n.1169T>C
ENST00000422986.6:c.*383T>C	ENSP00000393628.2:n.*383T>C
ENST00000595392.5:c.*228T>C	ENSP00000468912.1:n.*228T>C
ENST00000595952.5:c.598T>C	ENSP00000471155.1:p.Tyr200His
ENST00000596333.1:n.905T>C
ENST00000598145.1:c.729T>C
ENST00000601349.5:n.2006T>C
ENST00000601812.1:n.1159T>C
ENST00000617027.4:c.604T>C	ENSP00000483513.1:p.Tyr202His
NM_001030047.1:c.*452T>C	NP_001025218.1:n.*452T>C
NM_001030048.1:c.598T>C	NP_001025219.1:p.Tyr200His
NM_001648.2:c.727T>C MANE Select	NP_001639.1:p.Tyr243His
XM_011526923.1:c.745T>C	XP_011525225.1:p.Tyr249His
XR_935817.1:n.1324+814T>C