Canonical Allele Identifier: CA508200819

Gene: KLK3

Linked Data

• dbSNP Id: rs1255115588
• gnomAD v2: 19-51363305-G-T
• gnomAD v3: 19-50860049-G-T
• gnomAD v4: 19-50860049-G-T
• MyVariant Identifiers: chr19:g.51363305G>T (hg19) ; chr19:g.50860049G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860049G>T , CM000681.2:g.50860049G>T	GRCh38
NC_000019.9:g.51363305G>T , CM000681.1:g.51363305G>T	GRCh37
NC_000019.8:g.56055117G>T	NCBI36
NG_011653.1:g.10135G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.708G>T MANE Select	ENSP00000314151.1:p.Leu236=
ENST00000326003.6:c.708G>T	ENSP00000314151.1:p.Leu236=
ENST00000360617.7:c.1150G>T	ENSP00000353829.2:n.1150G>T
ENST00000422986.6:c.*364G>T	ENSP00000393628.2:n.*364G>T
ENST00000595392.5:c.*209G>T	ENSP00000468912.1:n.*209G>T
ENST00000595952.5:c.579G>T	ENSP00000471155.1:p.Leu193=
ENST00000596333.1:n.886G>T
ENST00000598145.1:c.710G>T
ENST00000601349.5:n.1987G>T
ENST00000601812.1:n.1140G>T
ENST00000617027.4:c.585G>T	ENSP00000483513.1:p.Leu195=
NM_001030047.1:c.*433G>T	NP_001025218.1:n.*433G>T
NM_001030048.1:c.579G>T	NP_001025219.1:p.Leu193=
NM_001648.2:c.708G>T MANE Select	NP_001639.1:p.Leu236=
XM_011526923.1:c.726G>T	XP_011525225.1:p.Leu242=
XR_935817.1:n.1324+795G>T