Canonical Allele Identifier: CA407025112

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363325A>T (hg19) ; chr19:g.50860069A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860069A>T , CM000681.2:g.50860069A>T	GRCh38
NC_000019.9:g.51363325A>T , CM000681.1:g.51363325A>T	GRCh37
NC_000019.8:g.56055137A>T	NCBI36
NG_011653.1:g.10155A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.728A>T MANE Select	ENSP00000314151.1:p.Tyr243Phe
ENST00000326003.6:c.728A>T	ENSP00000314151.1:p.Tyr243Phe
ENST00000360617.7:c.1170A>T	ENSP00000353829.2:n.1170A>T
ENST00000422986.6:c.*384A>T	ENSP00000393628.2:n.*384A>T
ENST00000595392.5:c.*229A>T	ENSP00000468912.1:n.*229A>T
ENST00000595952.5:c.599A>T	ENSP00000471155.1:p.Tyr200Phe
ENST00000596333.1:n.906A>T
ENST00000598145.1:c.730A>T
ENST00000601349.5:n.2007A>T
ENST00000601812.1:n.1160A>T
ENST00000617027.4:c.605A>T	ENSP00000483513.1:p.Tyr202Phe
NM_001030047.1:c.*453A>T	NP_001025218.1:n.*453A>T
NM_001030048.1:c.599A>T	NP_001025219.1:p.Tyr200Phe
NM_001648.2:c.728A>T MANE Select	NP_001639.1:p.Tyr243Phe
XM_011526923.1:c.746A>T	XP_011525225.1:p.Tyr249Phe
XR_935817.1:n.1324+815A>T