Canonical Allele Identifier: CA9604602

Gene: KLK3

Linked Data

• dbSNP Id: rs538660698
• ExAC: 19:51363333 G / T
• gnomAD v2: 19-51363333-G-T
• gnomAD v3: 19-50860077-G-T
• gnomAD v4: 19-50860077-G-T
• MyVariant Identifiers: chr19:g.51363333G>T (hg19) ; chr19:g.50860077G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860077G>T , CM000681.2:g.50860077G>T	GRCh38
NC_000019.9:g.51363333G>T , CM000681.1:g.51363333G>T	GRCh37
NC_000019.8:g.56055145G>T	NCBI36
NG_011653.1:g.10163G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.736G>T MANE Select	ENSP00000314151.1:p.Val246Leu
ENST00000326003.6:c.736G>T	ENSP00000314151.1:p.Val246Leu
ENST00000360617.7:c.1178G>T	ENSP00000353829.2:n.1178G>T
ENST00000422986.6:c.*392G>T	ENSP00000393628.2:n.*392G>T
ENST00000595392.5:c.*237G>T	ENSP00000468912.1:n.*237G>T
ENST00000595952.5:c.607G>T	ENSP00000471155.1:p.Val203Leu
ENST00000596333.1:n.914G>T
ENST00000598145.1:c.738G>T
ENST00000601349.5:n.2015G>T
ENST00000601812.1:n.1168G>T
ENST00000617027.4:c.613G>T	ENSP00000483513.1:p.Val205Leu
NM_001030047.1:c.*461G>T	NP_001025218.1:n.*461G>T
NM_001030048.1:c.607G>T	NP_001025219.1:p.Val203Leu
NM_001648.2:c.736G>T MANE Select	NP_001639.1:p.Val246Leu
XM_011526923.1:c.754G>T	XP_011525225.1:p.Val252Leu
XR_935817.1:n.1324+823G>T