Canonical Allele Identifier: CA407025037

Gene: KLK3

Linked Data

• dbSNP Id: rs372901531
• MyVariant Identifiers: chr19:g.51363309G>T (hg19) ; chr19:g.50860053G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860053G>T , CM000681.2:g.50860053G>T	GRCh38
NC_000019.9:g.51363309G>T , CM000681.1:g.51363309G>T	GRCh37
NC_000019.8:g.56055121G>T	NCBI36
NG_011653.1:g.10139G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.712G>T MANE Select	ENSP00000314151.1:p.Glu238Ter
ENST00000326003.6:c.712G>T	ENSP00000314151.1:p.Glu238Ter
ENST00000360617.7:c.1154G>T	ENSP00000353829.2:n.1154G>T
ENST00000422986.6:c.*368G>T	ENSP00000393628.2:n.*368G>T
ENST00000595392.5:c.*213G>T	ENSP00000468912.1:n.*213G>T
ENST00000595952.5:c.583G>T	ENSP00000471155.1:p.Glu195Ter
ENST00000596333.1:n.890G>T
ENST00000598145.1:c.714G>T
ENST00000601349.5:n.1991G>T
ENST00000601812.1:n.1144G>T
ENST00000617027.4:c.589G>T	ENSP00000483513.1:p.Glu197Ter
NM_001030047.1:c.*437G>T	NP_001025218.1:n.*437G>T
NM_001030048.1:c.583G>T	NP_001025219.1:p.Glu195Ter
NM_001648.2:c.712G>T MANE Select	NP_001639.1:p.Glu238Ter
XM_011526923.1:c.730G>T	XP_011525225.1:p.Glu244Ter
XR_935817.1:n.1324+799G>T