Canonical Allele Identifier: CA407025129

Gene: KLK3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.731C>T MANE Select	ENSP00000314151.1:p.Thr244Ile
ENST00000326003.6:c.731C>T	ENSP00000314151.1:p.Thr244Ile
ENST00000360617.7:c.1173C>T	ENSP00000353829.2:n.1173C>T
ENST00000422986.6:c.*387C>T	ENSP00000393628.2:n.*387C>T
ENST00000595392.5:c.*232C>T	ENSP00000468912.1:n.*232C>T
ENST00000595952.5:c.602C>T	ENSP00000471155.1:p.Thr201Ile
ENST00000596333.1:n.909C>T
ENST00000598145.1:c.733C>T
ENST00000601349.5:n.2010C>T
ENST00000601812.1:n.1163C>T
ENST00000617027.4:c.608C>T	ENSP00000483513.1:p.Thr203Ile
NM_001030047.1:c.*456C>T	NP_001025218.1:n.*456C>T
NM_001030048.1:c.602C>T	NP_001025219.1:p.Thr201Ile
NM_001648.2:c.731C>T MANE Select	NP_001639.1:p.Thr244Ile
XM_011526923.1:c.749C>T	XP_011525225.1:p.Thr250Ile
XR_935817.1:n.1324+818C>T