Canonical Allele Identifier: CA508313365

Gene: KLK3

Linked Data

• dbSNP Id: rs748662283
• gnomAD v2: 19-51361558-T-C
• gnomAD v4: 19-50858302-T-C
• MyVariant Identifiers: chr19:g.51361558T>C (hg19) ; chr19:g.50858302T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858302T>C , CM000681.2:g.50858302T>C	GRCh38
NC_000019.9:g.51361558T>C , CM000681.1:g.51361558T>C	GRCh37
NC_000019.8:g.56053370T>C	NCBI36
NG_011653.1:g.8388T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.480T>C MANE Select	ENSP00000314151.1:p.Ile160=
ENST00000326003.6:c.480T>C	ENSP00000314151.1:p.Ile160=
ENST00000360617.7:c.480T>C	ENSP00000353829.2:p.Ile160=
ENST00000422986.6:c.*136T>C	ENSP00000393628.2:n.*136T>C
ENST00000593997.5:c.480T>C	ENSP00000472907.1:p.Ile160=
ENST00000595392.5:c.356T>C	ENSP00000468912.1:p.Leu119Ser
ENST00000595952.5:c.351T>C	ENSP00000471155.1:p.Ile117=
ENST00000596185.5:c.*588T>C	ENSP00000471648.1:n.*588T>C
ENST00000596333.1:n.515T>C
ENST00000597286.5:c.369T>C	ENSP00000470523.1:p.Ile123=
ENST00000597483.5:c.351T>C	ENSP00000472411.1:p.Ile117=
ENST00000598145.1:c.464T>C
ENST00000601349.5:n.1759T>C
ENST00000601503.5:c.423T>C	ENSP00000472213.1:p.Ile141=
ENST00000601812.1:n.912T>C
ENST00000617027.4:c.357T>C	ENSP00000483513.1:p.Ile119=
NM_001030047.1:c.480T>C	NP_001025218.1:p.Ile160=
NM_001030048.1:c.351T>C	NP_001025219.1:p.Ile117=
NM_001648.2:c.480T>C MANE Select	NP_001639.1:p.Ile160=
XM_011526923.1:c.480T>C	XP_011525225.1:p.Ile160=
XM_011526924.1:c.480T>C	XP_011525226.1:p.Ile160=
XR_935817.1:n.515T>C