Canonical Allele Identifier: CA2127856148

Gene: AKAP6

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.32833732_32833736delinsTAAAG , CM000676.2:g.32833732_32833736delinsTAAAG	GRCh38
NC_000014.8:g.33302938_33302942delinsTAAAG , CM000676.1:g.33302938_33302942delinsTAAAG	GRCh37
NC_000014.7:g.32372689_32372693delinsTAAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000280979.9:c.*3927_*3931delinsTAAAG MANE Select	ENSP00000280979.4:n.*3927_*3931delinsTAAA...
ENST00000280979.8:c.*3927_*3931delinsTAAAG	ENSP00000280979.4:n.*3927_*3931delinsTAAA...
XM_005268219.3:c.*3927_*3931delinsTAAAG	XP_005268276.1:n.*3927_*3931delinsTAAAG
XM_011537378.1:c.*3927_*3931delinsTAAAG	XP_011535680.1:n.*3927_*3931delinsTAAAG
XM_011537379.1:c.*3927_*3931delinsTAAAG	XP_011535681.1:n.*3927_*3931delinsTAAAG
XM_011537380.1:c.*3927_*3931delinsTAAAG	XP_011535682.1:n.*3927_*3931delinsTAAAG
XM_011537381.1:c.*3927_*3931delinsTAAAG	XP_011535683.1:n.*3927_*3931delinsTAAAG
XM_011537382.1:c.*3927_*3931delinsTAAAG	XP_011535684.1:n.*3927_*3931delinsTAAAG
XM_011537383.1:c.*3927_*3931delinsTAAAG	XP_011535685.1:n.*3927_*3931delinsTAAAG
XM_017021808.2:c.*3927_*3931delinsTAAAG	XP_016877297.1:n.*3927_*3931delinsTAAAG
NM_004274.5:c.*3927_*3931delinsTAAAG MANE Select	NP_004265.3:n.*3927_*3931delinsTAAAG