Canonical Allele Identifier: CA407024820

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363229G>T (hg19) ; chr19:g.50859973G>T (hg38)
• PubMed: PMID:28135719

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50859973G>T , CM000681.2:g.50859973G>T	GRCh38
NC_000019.9:g.51363229G>T , CM000681.1:g.51363229G>T	GRCh37
NC_000019.8:g.56055041G>T	NCBI36
NG_011653.1:g.10059G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.632G>T MANE Select	ENSP00000314151.1:p.Gly211Val
ENST00000326003.6:c.632G>T	ENSP00000314151.1:p.Gly211Val
ENST00000360617.7:c.1074G>T	ENSP00000353829.2:n.1074G>T
ENST00000422986.6:c.*288G>T	ENSP00000393628.2:n.*288G>T
ENST00000595392.5:c.*133G>T	ENSP00000468912.1:n.*133G>T
ENST00000595952.5:c.503G>T	ENSP00000471155.1:p.Gly168Val
ENST00000596185.5:c.*740G>T	ENSP00000471648.1:n.*740G>T
ENST00000596333.1:n.810G>T
ENST00000598145.1:c.634G>T
ENST00000601349.5:n.1911G>T
ENST00000601812.1:n.1064G>T
ENST00000617027.4:c.509G>T	ENSP00000483513.1:p.Gly170Val
NM_001030047.1:c.*357G>T	NP_001025218.1:n.*357G>T
NM_001030048.1:c.503G>T	NP_001025219.1:p.Gly168Val
NM_001648.2:c.632G>T MANE Select	NP_001639.1:p.Gly211Val
XM_011526923.1:c.650G>T	XP_011525225.1:p.Gly217Val
XM_011526924.1:c.*357G>T	XP_011525226.1:n.*357G>T
XR_935817.1:n.1324+719G>T