Canonical Allele Identifier: CA407022791

Gene: KLK3

Linked Data

• gnomAD v4: 19-50858283-C-T
• MyVariant Identifiers: chr19:g.51361539C>T (hg19) ; chr19:g.50858283C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858283C>T , CM000681.2:g.50858283C>T	GRCh38
NC_000019.9:g.51361539C>T , CM000681.1:g.51361539C>T	GRCh37
NC_000019.8:g.56053351C>T	NCBI36
NG_011653.1:g.8369C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.461C>T MANE Select	ENSP00000314151.1:p.Ala154Val
ENST00000326003.6:c.461C>T	ENSP00000314151.1:p.Ala154Val
ENST00000360617.7:c.461C>T	ENSP00000353829.2:p.Ala154Val
ENST00000422986.6:c.*117C>T	ENSP00000393628.2:n.*117C>T
ENST00000593997.5:c.461C>T	ENSP00000472907.1:p.Ala154Val
ENST00000595392.5:c.353-16C>T	ENSP00000468912.1:n.353-16C>T
ENST00000595952.5:c.332C>T	ENSP00000471155.1:p.Ala111Val
ENST00000596185.5:c.*569C>T	ENSP00000471648.1:n.*569C>T
ENST00000596333.1:n.496C>T
ENST00000597286.5:c.350C>T	ENSP00000470523.1:p.Ala117Val
ENST00000597483.5:c.332C>T	ENSP00000472411.1:p.Ala111Val
ENST00000598145.1:c.445C>T
ENST00000601349.5:n.1740C>T
ENST00000601503.5:c.404C>T	ENSP00000472213.1:p.Ala135Val
ENST00000601812.1:n.893C>T
ENST00000617027.4:c.354-16C>T	ENSP00000483513.1:n.354-16C>T
NM_001030047.1:c.461C>T	NP_001025218.1:p.Ala154Val
NM_001030048.1:c.332C>T	NP_001025219.1:p.Ala111Val
NM_001648.2:c.461C>T MANE Select	NP_001639.1:p.Ala154Val
XM_011526923.1:c.461C>T	XP_011525225.1:p.Ala154Val
XM_011526924.1:c.461C>T	XP_011525226.1:p.Ala154Val
XR_935817.1:n.496C>T