Canonical Allele Identifier: CA407025086

Gene: KLK3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.722C>G MANE Select	ENSP00000314151.1:p.Ser241Cys
ENST00000326003.6:c.722C>G	ENSP00000314151.1:p.Ser241Cys
ENST00000360617.7:c.1164C>G	ENSP00000353829.2:n.1164C>G
ENST00000422986.6:c.*378C>G	ENSP00000393628.2:n.*378C>G
ENST00000595392.5:c.*223C>G	ENSP00000468912.1:n.*223C>G
ENST00000595952.5:c.593C>G	ENSP00000471155.1:p.Ser198Cys
ENST00000596333.1:n.900C>G
ENST00000598145.1:c.724C>G
ENST00000601349.5:n.2001C>G
ENST00000601812.1:n.1154C>G
ENST00000617027.4:c.599C>G	ENSP00000483513.1:p.Ser200Cys
NM_001030047.1:c.*447C>G	NP_001025218.1:n.*447C>G
NM_001030048.1:c.593C>G	NP_001025219.1:p.Ser198Cys
NM_001648.2:c.722C>G MANE Select	NP_001639.1:p.Ser241Cys
XM_011526923.1:c.740C>G	XP_011525225.1:p.Ser247Cys
XR_935817.1:n.1324+809C>G