Canonical Allele Identifier: CA407024876

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363257T>A (hg19) ; chr19:g.50860001T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860001T>A , CM000681.2:g.50860001T>A	GRCh38
NC_000019.9:g.51363257T>A , CM000681.1:g.51363257T>A	GRCh37
NC_000019.8:g.56055069T>A	NCBI36
NG_011653.1:g.10087T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.660T>A MANE Select	ENSP00000314151.1:p.Asn220Lys
ENST00000326003.6:c.660T>A	ENSP00000314151.1:p.Asn220Lys
ENST00000360617.7:c.1102T>A	ENSP00000353829.2:n.1102T>A
ENST00000422986.6:c.*316T>A	ENSP00000393628.2:n.*316T>A
ENST00000595392.5:c.*161T>A	ENSP00000468912.1:n.*161T>A
ENST00000595952.5:c.531T>A	ENSP00000471155.1:p.Asn177Lys
ENST00000596185.5:c.*768T>A	ENSP00000471648.1:n.*768T>A
ENST00000596333.1:n.838T>A
ENST00000598145.1:c.662T>A
ENST00000601349.5:n.1939T>A
ENST00000601812.1:n.1092T>A
ENST00000617027.4:c.537T>A	ENSP00000483513.1:p.Asn179Lys
NM_001030047.1:c.*385T>A	NP_001025218.1:n.*385T>A
NM_001030048.1:c.531T>A	NP_001025219.1:p.Asn177Lys
NM_001648.2:c.660T>A MANE Select	NP_001639.1:p.Asn220Lys
XM_011526923.1:c.678T>A	XP_011525225.1:p.Asn226Lys
XM_011526924.1:c.*385T>A	XP_011525226.1:n.*385T>A
XR_935817.1:n.1324+747T>A