Canonical Allele Identifier: CA309634014

Gene: KLK3

Linked Data

• dbSNP Id: rs929959346
• MyVariant Identifiers: chr19:g.51363362C>T (hg19) ; chr19:g.50860106C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860106C>T , CM000681.2:g.50860106C>T	GRCh38
NC_000019.9:g.51363362C>T , CM000681.1:g.51363362C>T	GRCh37
NC_000019.8:g.56055174C>T	NCBI36
NG_011653.1:g.10192C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.765C>T MANE Select	ENSP00000314151.1:p.Asp255=
ENST00000326003.6:c.765C>T	ENSP00000314151.1:p.Asp255=
ENST00000360617.7:c.1207C>T	ENSP00000353829.2:n.1207C>T
ENST00000422986.6:c.*421C>T	ENSP00000393628.2:n.*421C>T
ENST00000595392.5:c.*266C>T	ENSP00000468912.1:n.*266C>T
ENST00000595952.5:c.636C>T	ENSP00000471155.1:p.Asp212=
ENST00000596333.1:n.943C>T
ENST00000598145.1:c.767C>T
ENST00000601349.5:n.2044C>T
ENST00000601812.1:n.1197C>T
ENST00000617027.4:c.642C>T	ENSP00000483513.1:p.Asp214=
NM_001030047.1:c.*490C>T	NP_001025218.1:n.*490C>T
NM_001030048.1:c.636C>T	NP_001025219.1:p.Asp212=
NM_001648.2:c.765C>T MANE Select	NP_001639.1:p.Asp255=
XM_011526923.1:c.783C>T	XP_011525225.1:p.Asp261=
XR_935817.1:n.1324+852C>T