Canonical Allele Identifier: CA407025051

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363312A>T (hg19) ; chr19:g.50860056A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860056A>T , CM000681.2:g.50860056A>T	GRCh38
NC_000019.9:g.51363312A>T , CM000681.1:g.51363312A>T	GRCh37
NC_000019.8:g.56055124A>T	NCBI36
NG_011653.1:g.10142A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.715A>T MANE Select	ENSP00000314151.1:p.Arg239Trp
ENST00000326003.6:c.715A>T	ENSP00000314151.1:p.Arg239Trp
ENST00000360617.7:c.1157A>T	ENSP00000353829.2:n.1157A>T
ENST00000422986.6:c.*371A>T	ENSP00000393628.2:n.*371A>T
ENST00000595392.5:c.*216A>T	ENSP00000468912.1:n.*216A>T
ENST00000595952.5:c.586A>T	ENSP00000471155.1:p.Arg196Trp
ENST00000596333.1:n.893A>T
ENST00000598145.1:c.717A>T
ENST00000601349.5:n.1994A>T
ENST00000601812.1:n.1147A>T
ENST00000617027.4:c.592A>T	ENSP00000483513.1:p.Arg198Trp
NM_001030047.1:c.*440A>T	NP_001025218.1:n.*440A>T
NM_001030048.1:c.586A>T	NP_001025219.1:p.Arg196Trp
NM_001648.2:c.715A>T MANE Select	NP_001639.1:p.Arg239Trp
XM_011526923.1:c.733A>T	XP_011525225.1:p.Arg245Trp
XR_935817.1:n.1324+802A>T