Canonical Allele Identifier: CA2127856278

Gene: AKAP6

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.32833828_32833829delinsCT , CM000676.2:g.32833828_32833829delinsCT	GRCh38
NC_000014.8:g.33303034_33303035delinsCT , CM000676.1:g.33303034_33303035delinsCT	GRCh37
NC_000014.7:g.32372785_32372786delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280979.9:c.*4023_*4024delinsCT MANE Select	ENSP00000280979.4:n.*4023_*4024delinsCT
ENST00000280979.8:c.*4023_*4024delinsCT	ENSP00000280979.4:n.*4023_*4024delinsCT
XM_005268219.3:c.*4023_*4024delinsCT	XP_005268276.1:n.*4023_*4024delinsCT
XM_011537378.1:c.*4023_*4024delinsCT	XP_011535680.1:n.*4023_*4024delinsCT
XM_011537379.1:c.*4023_*4024delinsCT	XP_011535681.1:n.*4023_*4024delinsCT
XM_011537380.1:c.*4023_*4024delinsCT	XP_011535682.1:n.*4023_*4024delinsCT
XM_011537381.1:c.*4023_*4024delinsCT	XP_011535683.1:n.*4023_*4024delinsCT
XM_011537382.1:c.*4023_*4024delinsCT	XP_011535684.1:n.*4023_*4024delinsCT
XM_011537383.1:c.*4023_*4024delinsCT	XP_011535685.1:n.*4023_*4024delinsCT
XM_017021808.2:c.*4023_*4024delinsCT	XP_016877297.1:n.*4023_*4024delinsCT
NM_004274.5:c.*4023_*4024delinsCT MANE Select	NP_004265.3:n.*4023_*4024delinsCT