Canonical Allele Identifier: CA407025125

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363328C>A (hg19) ; chr19:g.50860072C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860072C>A , CM000681.2:g.50860072C>A	GRCh38
NC_000019.9:g.51363328C>A , CM000681.1:g.51363328C>A	GRCh37
NC_000019.8:g.56055140C>A	NCBI36
NG_011653.1:g.10158C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.731C>A MANE Select	ENSP00000314151.1:p.Thr244Asn
ENST00000326003.6:c.731C>A	ENSP00000314151.1:p.Thr244Asn
ENST00000360617.7:c.1173C>A	ENSP00000353829.2:n.1173C>A
ENST00000422986.6:c.*387C>A	ENSP00000393628.2:n.*387C>A
ENST00000595392.5:c.*232C>A	ENSP00000468912.1:n.*232C>A
ENST00000595952.5:c.602C>A	ENSP00000471155.1:p.Thr201Asn
ENST00000596333.1:n.909C>A
ENST00000598145.1:c.733C>A
ENST00000601349.5:n.2010C>A
ENST00000601812.1:n.1163C>A
ENST00000617027.4:c.608C>A	ENSP00000483513.1:p.Thr203Asn
NM_001030047.1:c.*456C>A	NP_001025218.1:n.*456C>A
NM_001030048.1:c.602C>A	NP_001025219.1:p.Thr201Asn
NM_001648.2:c.731C>A MANE Select	NP_001639.1:p.Thr244Asn
XM_011526923.1:c.749C>A	XP_011525225.1:p.Thr250Asn
XR_935817.1:n.1324+818C>A