Canonical Allele Identifier: CA407021949

Gene: KLK3

Linked Data

• gnomAD v4: 19-50858035-C-A
• MyVariant Identifiers: chr19:g.51361291C>A (hg19) ; chr19:g.50858035C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858035C>A , CM000681.2:g.50858035C>A	GRCh38
NC_000019.9:g.51361291C>A , CM000681.1:g.51361291C>A	GRCh37
NC_000019.8:g.56053103C>A	NCBI36
NG_011653.1:g.8121C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.213C>A MANE Select	ENSP00000314151.1:p.Ser71Arg
ENST00000326003.6:c.213C>A	ENSP00000314151.1:p.Ser71Arg
ENST00000360617.7:c.213C>A	ENSP00000353829.2:p.Ser71Arg
ENST00000422986.6:c.213C>A	ENSP00000393628.2:p.Ser71Arg
ENST00000593997.5:c.213C>A	ENSP00000472907.1:p.Ser71Arg
ENST00000595392.5:c.213C>A	ENSP00000468912.1:p.Ser71Arg
ENST00000595952.5:c.207-123C>A	ENSP00000471155.1:n.207-123C>A
ENST00000596185.5:c.*321C>A	ENSP00000471648.1:n.*321C>A
ENST00000596333.1:n.248C>A
ENST00000597286.5:c.102C>A	ENSP00000470523.1:p.Ser34Arg
ENST00000597483.5:c.207-123C>A	ENSP00000472411.1:n.207-123C>A
ENST00000598145.1:c.197C>A
ENST00000601349.5:n.1492C>A
ENST00000601503.5:c.156C>A	ENSP00000472213.1:p.Ser52Arg
ENST00000601812.1:n.645C>A
ENST00000617027.4:c.213C>A	ENSP00000483513.1:p.Ser71Arg
NM_001030047.1:c.213C>A	NP_001025218.1:p.Ser71Arg
NM_001030048.1:c.207-123C>A	NP_001025219.1:n.207-123C>A
NM_001648.2:c.213C>A MANE Select	NP_001639.1:p.Ser71Arg
XM_011526923.1:c.213C>A	XP_011525225.1:p.Ser71Arg
XM_011526924.1:c.213C>A	XP_011525226.1:p.Ser71Arg
XR_935817.1:n.248C>A