Canonical Allele Identifier: CA2127856149

Gene: AKAP6

Linked Data

• dbSNP Id: rs2034844718

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.32833736_32833739del , CM000676.2:g.32833736_32833739del	GRCh38
NC_000014.8:g.33302942_33302945del , CM000676.1:g.33302942_33302945del	GRCh37
NC_000014.7:g.32372693_32372696del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000280979.9:c.*3931_*3934del MANE Select	ENSP00000280979.4:n.*3931_*3934del
ENST00000280979.8:c.*3931_*3934del	ENSP00000280979.4:n.*3931_*3934del
XM_005268219.3:c.*3931_*3934del	XP_005268276.1:n.*3931_*3934del
XM_011537378.1:c.*3931_*3934del	XP_011535680.1:n.*3931_*3934del
XM_011537379.1:c.*3931_*3934del	XP_011535681.1:n.*3931_*3934del
XM_011537380.1:c.*3931_*3934del	XP_011535682.1:n.*3931_*3934del
XM_011537381.1:c.*3931_*3934del	XP_011535683.1:n.*3931_*3934del
XM_011537382.1:c.*3931_*3934del	XP_011535684.1:n.*3931_*3934del
XM_011537383.1:c.*3931_*3934del	XP_011535685.1:n.*3931_*3934del
XM_017021808.2:c.*3931_*3934del	XP_016877297.1:n.*3931_*3934del
NM_004274.5:c.*3931_*3934del MANE Select	NP_004265.3:n.*3931_*3934del