Canonical Allele Identifier: CA309634061

Gene: KLK3

Linked Data

• dbSNP Id: rs1008358932
• gnomAD v4: 19-50860147-A-G
• MyVariant Identifiers: chr19:g.51363403A>G (hg19) ; chr19:g.50860147A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860147A>G , CM000681.2:g.50860147A>G	GRCh38
NC_000019.9:g.51363403A>G , CM000681.1:g.51363403A>G	GRCh37
NC_000019.8:g.56055215A>G	NCBI36
NG_011653.1:g.10233A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.*20A>G MANE Select	ENSP00000314151.1:n.*20A>G
ENST00000326003.6:c.*20A>G	ENSP00000314151.1:n.*20A>G
ENST00000360617.7:c.1248A>G	ENSP00000353829.2:n.1248A>G
ENST00000422986.6:c.*462A>G	ENSP00000393628.2:n.*462A>G
ENST00000595392.5:c.*307A>G	ENSP00000468912.1:n.*307A>G
ENST00000595952.5:c.*20A>G	ENSP00000471155.1:n.*20A>G
ENST00000596333.1:n.984A>G
ENST00000598145.1:c.808A>G
ENST00000601349.5:n.2085A>G
ENST00000617027.4:c.*20A>G	ENSP00000483513.1:n.*20A>G
NM_001030047.1:c.*531A>G	NP_001025218.1:n.*531A>G
NM_001030048.1:c.*20A>G	NP_001025219.1:n.*20A>G
NM_001648.2:c.*20A>G MANE Select	NP_001639.1:n.*20A>G
XM_011526923.1:c.*20A>G	XP_011525225.1:n.*20A>G
XR_935817.1:n.1324+893A>G