Canonical Allele Identifier: CA407025012

Gene: KLK3

Linked Data

• COSMIC: COSM98305
• MyVariant Identifiers: chr19:g.51363301C>T (hg19) ; chr19:g.50860045C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860045C>T , CM000681.2:g.50860045C>T	GRCh38
NC_000019.9:g.51363301C>T , CM000681.1:g.51363301C>T	GRCh37
NC_000019.8:g.56055113C>T	NCBI36
NG_011653.1:g.10131C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.704C>T MANE Select	ENSP00000314151.1:p.Ala235Val
ENST00000326003.6:c.704C>T	ENSP00000314151.1:p.Ala235Val
ENST00000360617.7:c.1146C>T	ENSP00000353829.2:n.1146C>T
ENST00000422986.6:c.*360C>T	ENSP00000393628.2:n.*360C>T
ENST00000595392.5:c.*205C>T	ENSP00000468912.1:n.*205C>T
ENST00000595952.5:c.575C>T	ENSP00000471155.1:p.Ala192Val
ENST00000596333.1:n.882C>T
ENST00000598145.1:c.706C>T
ENST00000601349.5:n.1983C>T
ENST00000601812.1:n.1136C>T
ENST00000617027.4:c.581C>T	ENSP00000483513.1:p.Ala194Val
NM_001030047.1:c.*429C>T	NP_001025218.1:n.*429C>T
NM_001030048.1:c.575C>T	NP_001025219.1:p.Ala192Val
NM_001648.2:c.704C>T MANE Select	NP_001639.1:p.Ala235Val
XM_011526923.1:c.722C>T	XP_011525225.1:p.Ala241Val
XR_935817.1:n.1324+791C>T