Canonical Allele Identifier: CA2586639265

Gene: KLK3

Linked Data

• gnomAD v4: 19-50860152-A-AGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860153_50860154insCTG , CM000681.2:g.50860153_50860154insCTG	GRCh38
NC_000019.9:g.51363409_51363410insCTG , CM000681.1:g.51363409_51363410insCTG	GRCh37
NC_000019.8:g.56055221_56055222insCTG	NCBI36
NG_011653.1:g.10239_10240insCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000326003.7:c.*26_*27insCTG MANE Select	ENSP00000314151.1:n.*26_*27insCTG
ENST00000326003.6:c.*26_*27insCTG	ENSP00000314151.1:n.*26_*27insCTG
ENST00000360617.7:c.1254_1255insCTG	ENSP00000353829.2:n.1254_1255insCTG
ENST00000422986.6:c.*468_*469insCTG	ENSP00000393628.2:n.*468_*469insCTG
ENST00000595392.5:c.*313_*314insCTG	ENSP00000468912.1:n.*313_*314insCTG
ENST00000595952.5:c.*26_*27insCTG	ENSP00000471155.1:n.*26_*27insCTG
ENST00000596333.1:n.990_991insCTG
ENST00000598145.1:c.814_815insCTG
ENST00000601349.5:n.2091_2092insCTG
ENST00000617027.4:c.*26_*27insCTG	ENSP00000483513.1:n.*26_*27insCTG
NM_001030047.1:c.*537_*538insCTG	NP_001025218.1:n.*537_*538insCTG
NM_001030048.1:c.*26_*27insCTG	NP_001025219.1:n.*26_*27insCTG
NM_001648.2:c.*26_*27insCTG MANE Select	NP_001639.1:n.*26_*27insCTG
XM_011526923.1:c.*26_*27insCTG	XP_011525225.1:n.*26_*27insCTG
XR_935817.1:n.1324+899_1324+900insCTG