Canonical Allele Identifier: CA407024822

Gene: KLK3

Linked Data

• gnomAD v4: 19-50859973-G-A
• MyVariant Identifiers: chr19:g.51363229G>A (hg19) ; chr19:g.50859973G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50859973G>A , CM000681.2:g.50859973G>A	GRCh38
NC_000019.9:g.51363229G>A , CM000681.1:g.51363229G>A	GRCh37
NC_000019.8:g.56055041G>A	NCBI36
NG_011653.1:g.10059G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.632G>A MANE Select	ENSP00000314151.1:p.Gly211Asp
ENST00000326003.6:c.632G>A	ENSP00000314151.1:p.Gly211Asp
ENST00000360617.7:c.1074G>A	ENSP00000353829.2:n.1074G>A
ENST00000422986.6:c.*288G>A	ENSP00000393628.2:n.*288G>A
ENST00000595392.5:c.*133G>A	ENSP00000468912.1:n.*133G>A
ENST00000595952.5:c.503G>A	ENSP00000471155.1:p.Gly168Asp
ENST00000596185.5:c.*740G>A	ENSP00000471648.1:n.*740G>A
ENST00000596333.1:n.810G>A
ENST00000598145.1:c.634G>A
ENST00000601349.5:n.1911G>A
ENST00000601812.1:n.1064G>A
ENST00000617027.4:c.509G>A	ENSP00000483513.1:p.Gly170Asp
NM_001030047.1:c.*357G>A	NP_001025218.1:n.*357G>A
NM_001030048.1:c.503G>A	NP_001025219.1:p.Gly168Asp
NM_001648.2:c.632G>A MANE Select	NP_001639.1:p.Gly211Asp
XM_011526923.1:c.650G>A	XP_011525225.1:p.Gly217Asp
XM_011526924.1:c.*357G>A	XP_011525226.1:n.*357G>A
XR_935817.1:n.1324+719G>A