Canonical Allele Identifier: CA508200849

Gene: KLK3

Linked Data

• COSMIC: COSM3725449
• MyVariant Identifiers: chr19:g.51363356C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860100C>A , CM000681.2:g.50860100C>A	GRCh38
NC_000019.9:g.51363356C>A , CM000681.1:g.51363356C>A	GRCh37
NC_000019.8:g.56055168C>A	NCBI36
NG_011653.1:g.10186C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.759C>A MANE Select	ENSP00000314151.1:p.Ile253=
ENST00000326003.6:c.759C>A	ENSP00000314151.1:p.Ile253=
ENST00000360617.7:c.1201C>A	ENSP00000353829.2:n.1201C>A
ENST00000422986.6:c.*415C>A	ENSP00000393628.2:n.*415C>A
ENST00000595392.5:c.*260C>A	ENSP00000468912.1:n.*260C>A
ENST00000595952.5:c.630C>A	ENSP00000471155.1:p.Ile210=
ENST00000596333.1:n.937C>A
ENST00000598145.1:c.761C>A
ENST00000601349.5:n.2038C>A
ENST00000601812.1:n.1191C>A
ENST00000617027.4:c.636C>A	ENSP00000483513.1:p.Ile212=
NM_001030047.1:c.*484C>A	NP_001025218.1:n.*484C>A
NM_001030048.1:c.630C>A	NP_001025219.1:p.Ile210=
NM_001648.2:c.759C>A MANE Select	NP_001639.1:p.Ile253=
XM_011526923.1:c.777C>A	XP_011525225.1:p.Ile259=
XR_935817.1:n.1324+846C>A