Canonical Allele Identifier: CA2127856110

Gene: AKAP6

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.32833676_32833677delinsGT , CM000676.2:g.32833676_32833677delinsGT	GRCh38
NC_000014.8:g.33302882_33302883delinsGT , CM000676.1:g.33302882_33302883delinsGT	GRCh37
NC_000014.7:g.32372633_32372634delinsGT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000280979.9:c.*3871_*3872delinsGT MANE Select	ENSP00000280979.4:n.*3871_*3872delinsGT
ENST00000280979.8:c.*3871_*3872delinsGT	ENSP00000280979.4:n.*3871_*3872delinsGT
XM_005268219.3:c.*3871_*3872delinsGT	XP_005268276.1:n.*3871_*3872delinsGT
XM_011537378.1:c.*3871_*3872delinsGT	XP_011535680.1:n.*3871_*3872delinsGT
XM_011537379.1:c.*3871_*3872delinsGT	XP_011535681.1:n.*3871_*3872delinsGT
XM_011537380.1:c.*3871_*3872delinsGT	XP_011535682.1:n.*3871_*3872delinsGT
XM_011537381.1:c.*3871_*3872delinsGT	XP_011535683.1:n.*3871_*3872delinsGT
XM_011537382.1:c.*3871_*3872delinsGT	XP_011535684.1:n.*3871_*3872delinsGT
XM_011537383.1:c.*3871_*3872delinsGT	XP_011535685.1:n.*3871_*3872delinsGT
XM_017021808.2:c.*3871_*3872delinsGT	XP_016877297.1:n.*3871_*3872delinsGT
NM_004274.5:c.*3871_*3872delinsGT MANE Select	NP_004265.3:n.*3871_*3872delinsGT