Canonical Allele Identifier: CA633899633

Gene: KLK3

Linked Data

• dbSNP Id: rs1348001094
• gnomAD v2: 19-51363219-T-TA
• gnomAD v4: 19-50859963-T-TA
• MyVariant Identifiers: chr19:g.51363219_51363220insA (hg19) ; chr19:g.50859963_50859964insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50859964dup , CM000681.2:g.50859964dup	GRCh38
NC_000019.9:g.51363220dup , CM000681.1:g.51363220dup	GRCh37
NC_000019.8:g.56055032dup	NCBI36
NG_011653.1:g.10050dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.631-8dup MANE Select	ENSP00000314151.1:n.631-8dup
ENST00000326003.6:c.631-8dup	ENSP00000314151.1:n.631-8dup
ENST00000360617.7:c.1065dup	ENSP00000353829.2:n.1065dup
ENST00000422986.6:c.*287-8dup	ENSP00000393628.2:n.*287-8dup
ENST00000595392.5:c.*132-8dup	ENSP00000468912.1:n.*132-8dup
ENST00000595952.5:c.502-8dup	ENSP00000471155.1:n.502-8dup
ENST00000596185.5:c.*739-8dup	ENSP00000471648.1:n.*739-8dup
ENST00000596333.1:n.809-8dup
ENST00000598145.1:c.633-8dup
ENST00000601349.5:n.1910-8dup
ENST00000601812.1:n.1063-8dup
ENST00000617027.4:c.508-8dup	ENSP00000483513.1:n.508-8dup
NM_001030047.1:c.*348dup	NP_001025218.1:n.*348dup
NM_001030048.1:c.502-8dup	NP_001025219.1:n.502-8dup
NM_001648.2:c.631-8dup MANE Select	NP_001639.1:n.631-8dup
XM_011526923.1:c.649-8dup	XP_011525225.1:n.649-8dup
XM_011526924.1:c.*348dup	XP_011525226.1:n.*348dup
XR_935817.1:n.1324+710dup