Canonical Allele Identifier: CA508200847

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363347G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860091G>T , CM000681.2:g.50860091G>T	GRCh38
NC_000019.9:g.51363347G>T , CM000681.1:g.51363347G>T	GRCh37
NC_000019.8:g.56055159G>T	NCBI36
NG_011653.1:g.10177G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.750G>T MANE Select	ENSP00000314151.1:p.Arg250=
ENST00000326003.6:c.750G>T	ENSP00000314151.1:p.Arg250=
ENST00000360617.7:c.1192G>T	ENSP00000353829.2:n.1192G>T
ENST00000422986.6:c.*406G>T	ENSP00000393628.2:n.*406G>T
ENST00000595392.5:c.*251G>T	ENSP00000468912.1:n.*251G>T
ENST00000595952.5:c.621G>T	ENSP00000471155.1:p.Arg207=
ENST00000596333.1:n.928G>T
ENST00000598145.1:c.752G>T
ENST00000601349.5:n.2029G>T
ENST00000601812.1:n.1182G>T
ENST00000617027.4:c.627G>T	ENSP00000483513.1:p.Arg209=
NM_001030047.1:c.*475G>T	NP_001025218.1:n.*475G>T
NM_001030048.1:c.621G>T	NP_001025219.1:p.Arg207=
NM_001648.2:c.750G>T MANE Select	NP_001639.1:p.Arg250=
XM_011526923.1:c.768G>T	XP_011525225.1:p.Arg256=
XR_935817.1:n.1324+837G>T