Canonical Allele Identifier: CA2586639248

Gene: KLK3

Linked Data

• gnomAD v4: 19-50860417-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860417_50860418insC , CM000681.2:g.50860417_50860418insC	GRCh38
NC_000019.9:g.51363673_51363674insC , CM000681.1:g.51363673_51363674insC	GRCh37
NC_000019.8:g.56055485_56055486insC	NCBI36
NG_011653.1:g.10503_10504insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.*290_*291insC MANE Select	ENSP00000314151.1:n.*290_*291insC
ENST00000326003.6:c.*290_*291insC	ENSP00000314151.1:n.*290_*291insC
ENST00000360617.7:c.1518_1519insC	ENSP00000353829.2:n.1518_1519insC
ENST00000422986.6:c.*732_*733insC	ENSP00000393628.2:n.*732_*733insC
ENST00000595952.5:c.*290_*291insC	ENSP00000471155.1:n.*290_*291insC
ENST00000596333.1:n.1254_1255insC
ENST00000601349.5:n.2355_2356insC
ENST00000617027.4:c.*290_*291insC	ENSP00000483513.1:n.*290_*291insC
NM_001030047.1:c.*801_*802insC	NP_001025218.1:n.*801_*802insC
NM_001030048.1:c.*290_*291insC	NP_001025219.1:n.*290_*291insC
NM_001648.2:c.*290_*291insC MANE Select	NP_001639.1:n.*290_*291insC
XM_011526923.1:c.*290_*291insC	XP_011525225.1:n.*290_*291insC
XR_935817.1:n.1324+1163_1324+1164insC