Canonical Allele Identifier: CA2538942632
Gene: AKAP6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.32833715G>A , CM000676.2:g.32833715G>A GRCh38
NC_000014.8:g.33302921G>A , CM000676.1:g.33302921G>A GRCh37
NC_000014.7:g.32372672G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000280979.9:c.*3910G>A MANE Select ENSP00000280979.4:n.*3910G>A
ENST00000280979.8:c.*3910G>A ENSP00000280979.4:n.*3910G>A
XM_005268219.3:c.*3910G>A XP_005268276.1:n.*3910G>A
XM_011537378.1:c.*3910G>A XP_011535680.1:n.*3910G>A
XM_011537379.1:c.*3910G>A XP_011535681.1:n.*3910G>A
XM_011537380.1:c.*3910G>A XP_011535682.1:n.*3910G>A
XM_011537381.1:c.*3910G>A XP_011535683.1:n.*3910G>A
XM_011537382.1:c.*3910G>A XP_011535684.1:n.*3910G>A
XM_011537383.1:c.*3910G>A XP_011535685.1:n.*3910G>A
XM_017021808.2:c.*3910G>A XP_016877297.1:n.*3910G>A
NM_004274.5:c.*3910G>A MANE Select NP_004265.3:n.*3910G>A
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