Canonical Allele Identifier: CA2127856111
Gene: AKAP6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.32833683A= , CM000676.2:g.32833683A= GRCh38
NC_000014.8:g.33302889A= , CM000676.1:g.33302889A= GRCh37
NC_000014.7:g.32372640A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000280979.9:c.*3878A= MANE Select ENSP00000280979.4:n.*3878A=
ENST00000280979.8:c.*3878A= ENSP00000280979.4:n.*3878A=
XM_005268219.3:c.*3878A= XP_005268276.1:n.*3878A=
XM_011537378.1:c.*3878A= XP_011535680.1:n.*3878A=
XM_011537379.1:c.*3878A= XP_011535681.1:n.*3878A=
XM_011537380.1:c.*3878A= XP_011535682.1:n.*3878A=
XM_011537381.1:c.*3878A= XP_011535683.1:n.*3878A=
XM_011537382.1:c.*3878A= XP_011535684.1:n.*3878A=
XM_011537383.1:c.*3878A= XP_011535685.1:n.*3878A=
XM_017021808.2:c.*3878A= XP_016877297.1:n.*3878A=
NM_004274.5:c.*3878A= MANE Select NP_004265.3:n.*3878A=