Canonical Allele Identifier: CA2624504784
Gene: AKAP6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.32833828C>A , CM000676.2:g.32833828C>A GRCh38
NC_000014.8:g.33303034C>A , CM000676.1:g.33303034C>A GRCh37
NC_000014.7:g.32372785C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000280979.9:c.*4023C>A MANE Select ENSP00000280979.4:n.*4023C>A
ENST00000280979.8:c.*4023C>A ENSP00000280979.4:n.*4023C>A
XM_005268219.3:c.*4023C>A XP_005268276.1:n.*4023C>A
XM_011537378.1:c.*4023C>A XP_011535680.1:n.*4023C>A
XM_011537379.1:c.*4023C>A XP_011535681.1:n.*4023C>A
XM_011537380.1:c.*4023C>A XP_011535682.1:n.*4023C>A
XM_011537381.1:c.*4023C>A XP_011535683.1:n.*4023C>A
XM_011537382.1:c.*4023C>A XP_011535684.1:n.*4023C>A
XM_011537383.1:c.*4023C>A XP_011535685.1:n.*4023C>A
XM_017021808.2:c.*4023C>A XP_016877297.1:n.*4023C>A
NM_004274.5:c.*4023C>A MANE Select NP_004265.3:n.*4023C>A