Canonical Allele Identifier: CA407025004

Gene: KLK3

Linked Data

• dbSNP Id: rs1313860800
• MyVariant Identifiers: chr19:g.51363300G>T (hg19) ; chr19:g.50860044G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860044G>T , CM000681.2:g.50860044G>T	GRCh38
NC_000019.9:g.51363300G>T , CM000681.1:g.51363300G>T	GRCh37
NC_000019.8:g.56055112G>T	NCBI36
NG_011653.1:g.10130G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.703G>T MANE Select	ENSP00000314151.1:p.Ala235Ser
ENST00000326003.6:c.703G>T	ENSP00000314151.1:p.Ala235Ser
ENST00000360617.7:c.1145G>T	ENSP00000353829.2:n.1145G>T
ENST00000422986.6:c.*359G>T	ENSP00000393628.2:n.*359G>T
ENST00000595392.5:c.*204G>T	ENSP00000468912.1:n.*204G>T
ENST00000595952.5:c.574G>T	ENSP00000471155.1:p.Ala192Ser
ENST00000596333.1:n.881G>T
ENST00000598145.1:c.705G>T
ENST00000601349.5:n.1982G>T
ENST00000601812.1:n.1135G>T
ENST00000617027.4:c.580G>T	ENSP00000483513.1:p.Ala194Ser
NM_001030047.1:c.*428G>T	NP_001025218.1:n.*428G>T
NM_001030048.1:c.574G>T	NP_001025219.1:p.Ala192Ser
NM_001648.2:c.703G>T MANE Select	NP_001639.1:p.Ala235Ser
XM_011526923.1:c.721G>T	XP_011525225.1:p.Ala241Ser
XR_935817.1:n.1324+790G>T