Canonical Allele Identifier: CA508200824

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363314G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860058G>A , CM000681.2:g.50860058G>A	GRCh38
NC_000019.9:g.51363314G>A , CM000681.1:g.51363314G>A	GRCh37
NC_000019.8:g.56055126G>A	NCBI36
NG_011653.1:g.10144G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.717G>A MANE Select	ENSP00000314151.1:p.Arg239=
ENST00000326003.6:c.717G>A	ENSP00000314151.1:p.Arg239=
ENST00000360617.7:c.1159G>A	ENSP00000353829.2:n.1159G>A
ENST00000422986.6:c.*373G>A	ENSP00000393628.2:n.*373G>A
ENST00000595392.5:c.*218G>A	ENSP00000468912.1:n.*218G>A
ENST00000595952.5:c.588G>A	ENSP00000471155.1:p.Arg196=
ENST00000596333.1:n.895G>A
ENST00000598145.1:c.719G>A
ENST00000601349.5:n.1996G>A
ENST00000601812.1:n.1149G>A
ENST00000617027.4:c.594G>A	ENSP00000483513.1:p.Arg198=
NM_001030047.1:c.*442G>A	NP_001025218.1:n.*442G>A
NM_001030048.1:c.588G>A	NP_001025219.1:p.Arg196=
NM_001648.2:c.717G>A MANE Select	NP_001639.1:p.Arg239=
XM_011526923.1:c.735G>A	XP_011525225.1:p.Arg245=
XR_935817.1:n.1324+804G>A