Canonical Allele Identifier: CA508200841

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363338G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860082G>C , CM000681.2:g.50860082G>C	GRCh38
NC_000019.9:g.51363338G>C , CM000681.1:g.51363338G>C	GRCh37
NC_000019.8:g.56055150G>C	NCBI36
NG_011653.1:g.10168G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.741G>C MANE Select	ENSP00000314151.1:p.Val247=
ENST00000326003.6:c.741G>C	ENSP00000314151.1:p.Val247=
ENST00000360617.7:c.1183G>C	ENSP00000353829.2:n.1183G>C
ENST00000422986.6:c.*397G>C	ENSP00000393628.2:n.*397G>C
ENST00000595392.5:c.*242G>C	ENSP00000468912.1:n.*242G>C
ENST00000595952.5:c.612G>C	ENSP00000471155.1:p.Val204=
ENST00000596333.1:n.919G>C
ENST00000598145.1:c.743G>C
ENST00000601349.5:n.2020G>C
ENST00000601812.1:n.1173G>C
ENST00000617027.4:c.618G>C	ENSP00000483513.1:p.Val206=
NM_001030047.1:c.*466G>C	NP_001025218.1:n.*466G>C
NM_001030048.1:c.612G>C	NP_001025219.1:p.Val204=
NM_001648.2:c.741G>C MANE Select	NP_001639.1:p.Val247=
XM_011526923.1:c.759G>C	XP_011525225.1:p.Val253=
XR_935817.1:n.1324+828G>C