Canonical Allele Identifier: CA961726749
Gene: AKAP6 HGNC NCBI

Linked Data

dbSNP Id: rs2034843925

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.32833612T>C , CM000676.2:g.32833612T>C GRCh38
NC_000014.8:g.33302818T>C , CM000676.1:g.33302818T>C GRCh37
NC_000014.7:g.32372569T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000280979.9:c.*3807T>C MANE Select ENSP00000280979.4:n.*3807T>C
ENST00000280979.8:c.*3807T>C ENSP00000280979.4:n.*3807T>C
XM_005268219.3:c.*3807T>C XP_005268276.1:n.*3807T>C
XM_011537378.1:c.*3807T>C XP_011535680.1:n.*3807T>C
XM_011537379.1:c.*3807T>C XP_011535681.1:n.*3807T>C
XM_011537380.1:c.*3807T>C XP_011535682.1:n.*3807T>C
XM_011537381.1:c.*3807T>C XP_011535683.1:n.*3807T>C
XM_011537382.1:c.*3807T>C XP_011535684.1:n.*3807T>C
XM_011537383.1:c.*3807T>C XP_011535685.1:n.*3807T>C
XM_017021808.2:c.*3807T>C XP_016877297.1:n.*3807T>C
NM_004274.5:c.*3807T>C MANE Select NP_004265.3:n.*3807T>C