Canonical Allele Identifier: CA9604448

Gene: KLK3

Linked Data

• dbSNP Id: rs752696686
• ExAC: 19:51361578 C / T
• gnomAD v2: 19-51361578-C-T
• gnomAD v4: 19-50858322-C-T
• MyVariant Identifiers: chr19:g.51361578C>T (hg19) ; chr19:g.50858322C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858322C>T , CM000681.2:g.50858322C>T	GRCh38
NC_000019.9:g.51361578C>T , CM000681.1:g.51361578C>T	GRCh37
NC_000019.8:g.56053390C>T	NCBI36
NG_011653.1:g.8408C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.493+7C>T MANE Select	ENSP00000314151.1:n.493+7C>T
ENST00000326003.6:c.493+7C>T	ENSP00000314151.1:n.493+7C>T
ENST00000360617.7:c.493+7C>T	ENSP00000353829.2:n.493+7C>T
ENST00000422986.6:c.*149+7C>T	ENSP00000393628.2:n.*149+7C>T
ENST00000593997.5:c.493+7C>T	ENSP00000472907.1:n.493+7C>T
ENST00000595392.5:c.369+7C>T	ENSP00000468912.1:n.369+7C>T
ENST00000595952.5:c.364+7C>T	ENSP00000471155.1:n.364+7C>T
ENST00000596185.5:c.*601+7C>T	ENSP00000471648.1:n.*601+7C>T
ENST00000596333.1:n.535C>T
ENST00000597286.5:c.382+7C>T	ENSP00000470523.1:n.382+7C>T
ENST00000597483.5:c.364+7C>T	ENSP00000472411.1:n.364+7C>T
ENST00000598145.1:c.484C>T
ENST00000601349.5:n.1772+7C>T
ENST00000601503.5:c.436+7C>T	ENSP00000472213.1:n.436+7C>T
ENST00000601812.1:n.925+7C>T
ENST00000617027.4:c.370+7C>T	ENSP00000483513.1:n.370+7C>T
NM_001030047.1:c.493+7C>T	NP_001025218.1:n.493+7C>T
NM_001030048.1:c.364+7C>T	NP_001025219.1:n.364+7C>T
NM_001648.2:c.493+7C>T MANE Select	NP_001639.1:n.493+7C>T
XM_011526923.1:c.500C>T	XP_011525225.1:p.Pro167Leu
XM_011526924.1:c.500C>T	XP_011525226.1:p.Pro167Leu
XR_935817.1:n.528+7C>T