Canonical Allele Identifier: CA2127856224
Gene: AKAP6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.32833791C= , CM000676.2:g.32833791C= GRCh38
NC_000014.8:g.33302997C= , CM000676.1:g.33302997C= GRCh37
NC_000014.7:g.32372748C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000280979.9:c.*3986C= MANE Select ENSP00000280979.4:n.*3986C=
ENST00000280979.8:c.*3986C= ENSP00000280979.4:n.*3986C=
XM_005268219.3:c.*3986C= XP_005268276.1:n.*3986C=
XM_011537378.1:c.*3986C= XP_011535680.1:n.*3986C=
XM_011537379.1:c.*3986C= XP_011535681.1:n.*3986C=
XM_011537380.1:c.*3986C= XP_011535682.1:n.*3986C=
XM_011537381.1:c.*3986C= XP_011535683.1:n.*3986C=
XM_011537382.1:c.*3986C= XP_011535684.1:n.*3986C=
XM_011537383.1:c.*3986C= XP_011535685.1:n.*3986C=
XM_017021808.2:c.*3986C= XP_016877297.1:n.*3986C=
NM_004274.5:c.*3986C= MANE Select NP_004265.3:n.*3986C=