Canonical Allele Identifier: CA508200818

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363305G>C (hg19)

Genomic Alleles

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

Transcript Alleles

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