Canonical Allele Identifier: CA407025216

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363364C>A (hg19) ; chr19:g.50860108C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860108C>A , CM000681.2:g.50860108C>A	GRCh38
NC_000019.9:g.51363364C>A , CM000681.1:g.51363364C>A	GRCh37
NC_000019.8:g.56055176C>A	NCBI36
NG_011653.1:g.10194C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.767C>A MANE Select	ENSP00000314151.1:p.Thr256Asn
ENST00000326003.6:c.767C>A	ENSP00000314151.1:p.Thr256Asn
ENST00000360617.7:c.1209C>A	ENSP00000353829.2:n.1209C>A
ENST00000422986.6:c.*423C>A	ENSP00000393628.2:n.*423C>A
ENST00000595392.5:c.*268C>A	ENSP00000468912.1:n.*268C>A
ENST00000595952.5:c.638C>A	ENSP00000471155.1:p.Thr213Asn
ENST00000596333.1:n.945C>A
ENST00000598145.1:c.769C>A
ENST00000601349.5:n.2046C>A
ENST00000601812.1:n.1199C>A
ENST00000617027.4:c.644C>A	ENSP00000483513.1:p.Thr215Asn
NM_001030047.1:c.*492C>A	NP_001025218.1:n.*492C>A
NM_001030048.1:c.638C>A	NP_001025219.1:p.Thr213Asn
NM_001648.2:c.767C>A MANE Select	NP_001639.1:p.Thr256Asn
XM_011526923.1:c.785C>A	XP_011525225.1:p.Thr262Asn
XR_935817.1:n.1324+854C>A