Canonical Allele Identifier: CA407022715

Gene: KLK3

Linked Data

• dbSNP Id: rs1360908662
• gnomAD v2: 19-51361506-C-T
• gnomAD v4: 19-50858250-C-T
• MyVariant Identifiers: chr19:g.51361506C>T (hg19) ; chr19:g.50858250C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50858250C>T , CM000681.2:g.50858250C>T	GRCh38
NC_000019.9:g.51361506C>T , CM000681.1:g.51361506C>T	GRCh37
NC_000019.8:g.56053318C>T	NCBI36
NG_011653.1:g.8336C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.428C>T MANE Select	ENSP00000314151.1:p.Thr143Ile
ENST00000326003.6:c.428C>T	ENSP00000314151.1:p.Thr143Ile
ENST00000360617.7:c.428C>T	ENSP00000353829.2:p.Thr143Ile
ENST00000422986.6:c.*84C>T	ENSP00000393628.2:n.*84C>T
ENST00000593997.5:c.428C>T	ENSP00000472907.1:p.Thr143Ile
ENST00000595392.5:c.353-49C>T	ENSP00000468912.1:n.353-49C>T
ENST00000595952.5:c.299C>T	ENSP00000471155.1:p.Thr100Ile
ENST00000596185.5:c.*536C>T	ENSP00000471648.1:n.*536C>T
ENST00000596333.1:n.463C>T
ENST00000597286.5:c.317C>T	ENSP00000470523.1:p.Thr106Ile
ENST00000597483.5:c.299C>T	ENSP00000472411.1:p.Thr100Ile
ENST00000598145.1:c.412C>T
ENST00000601349.5:n.1707C>T
ENST00000601503.5:c.371C>T	ENSP00000472213.1:p.Thr124Ile
ENST00000601812.1:n.860C>T
ENST00000617027.4:c.354-49C>T	ENSP00000483513.1:n.354-49C>T
NM_001030047.1:c.428C>T	NP_001025218.1:p.Thr143Ile
NM_001030048.1:c.299C>T	NP_001025219.1:p.Thr100Ile
NM_001648.2:c.428C>T MANE Select	NP_001639.1:p.Thr143Ile
XM_011526923.1:c.428C>T	XP_011525225.1:p.Thr143Ile
XM_011526924.1:c.428C>T	XP_011525226.1:p.Thr143Ile
XR_935817.1:n.463C>T