Canonical Allele Identifier: CA407025088

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363319C>A (hg19) ; chr19:g.50860063C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860063C>A , CM000681.2:g.50860063C>A	GRCh38
NC_000019.9:g.51363319C>A , CM000681.1:g.51363319C>A	GRCh37
NC_000019.8:g.56055131C>A	NCBI36
NG_011653.1:g.10149C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.722C>A MANE Select	ENSP00000314151.1:p.Ser241Tyr
ENST00000326003.6:c.722C>A	ENSP00000314151.1:p.Ser241Tyr
ENST00000360617.7:c.1164C>A	ENSP00000353829.2:n.1164C>A
ENST00000422986.6:c.*378C>A	ENSP00000393628.2:n.*378C>A
ENST00000595392.5:c.*223C>A	ENSP00000468912.1:n.*223C>A
ENST00000595952.5:c.593C>A	ENSP00000471155.1:p.Ser198Tyr
ENST00000596333.1:n.900C>A
ENST00000598145.1:c.724C>A
ENST00000601349.5:n.2001C>A
ENST00000601812.1:n.1154C>A
ENST00000617027.4:c.599C>A	ENSP00000483513.1:p.Ser200Tyr
NM_001030047.1:c.*447C>A	NP_001025218.1:n.*447C>A
NM_001030048.1:c.593C>A	NP_001025219.1:p.Ser198Tyr
NM_001648.2:c.722C>A MANE Select	NP_001639.1:p.Ser241Tyr
XM_011526923.1:c.740C>A	XP_011525225.1:p.Ser247Tyr
XR_935817.1:n.1324+809C>A