Canonical Allele Identifier: CA407025047

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363311A>T (hg19) ; chr19:g.50860055A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860055A>T , CM000681.2:g.50860055A>T	GRCh38
NC_000019.9:g.51363311A>T , CM000681.1:g.51363311A>T	GRCh37
NC_000019.8:g.56055123A>T	NCBI36
NG_011653.1:g.10141A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.714A>T MANE Select	ENSP00000314151.1:p.Glu238Asp
ENST00000326003.6:c.714A>T	ENSP00000314151.1:p.Glu238Asp
ENST00000360617.7:c.1156A>T	ENSP00000353829.2:n.1156A>T
ENST00000422986.6:c.*370A>T	ENSP00000393628.2:n.*370A>T
ENST00000595392.5:c.*215A>T	ENSP00000468912.1:n.*215A>T
ENST00000595952.5:c.585A>T	ENSP00000471155.1:p.Glu195Asp
ENST00000596333.1:n.892A>T
ENST00000598145.1:c.716A>T
ENST00000601349.5:n.1993A>T
ENST00000601812.1:n.1146A>T
ENST00000617027.4:c.591A>T	ENSP00000483513.1:p.Glu197Asp
NM_001030047.1:c.*439A>T	NP_001025218.1:n.*439A>T
NM_001030048.1:c.585A>T	NP_001025219.1:p.Glu195Asp
NM_001648.2:c.714A>T MANE Select	NP_001639.1:p.Glu238Asp
XM_011526923.1:c.732A>T	XP_011525225.1:p.Glu244Asp
XR_935817.1:n.1324+801A>T