Canonical Allele Identifier: CA407024919

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363277C>A (hg19) ; chr19:g.50860021C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860021C>A , CM000681.2:g.50860021C>A	GRCh38
NC_000019.9:g.51363277C>A , CM000681.1:g.51363277C>A	GRCh37
NC_000019.8:g.56055089C>A	NCBI36
NG_011653.1:g.10107C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.680C>A MANE Select	ENSP00000314151.1:p.Thr227Lys
ENST00000326003.6:c.680C>A	ENSP00000314151.1:p.Thr227Lys
ENST00000360617.7:c.1122C>A	ENSP00000353829.2:n.1122C>A
ENST00000422986.6:c.*336C>A	ENSP00000393628.2:n.*336C>A
ENST00000595392.5:c.*181C>A	ENSP00000468912.1:n.*181C>A
ENST00000595952.5:c.551C>A	ENSP00000471155.1:p.Thr184Lys
ENST00000596333.1:n.858C>A
ENST00000598145.1:c.682C>A
ENST00000601349.5:n.1959C>A
ENST00000601812.1:n.1112C>A
ENST00000617027.4:c.557C>A	ENSP00000483513.1:p.Thr186Lys
NM_001030047.1:c.*405C>A	NP_001025218.1:n.*405C>A
NM_001030048.1:c.551C>A	NP_001025219.1:p.Thr184Lys
NM_001648.2:c.680C>A MANE Select	NP_001639.1:p.Thr227Lys
XM_011526923.1:c.698C>A	XP_011525225.1:p.Thr233Lys
XR_935817.1:n.1324+767C>A