Canonical Allele Identifier: CA2127859662
Gene: AKAP6 HGNC NCBI

Linked Data

dbSNP Id: rs2383378

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.32813264C>G , CM000676.2:g.32813264C>G GRCh38
NC_000014.8:g.33282470C>G , CM000676.1:g.33282470C>G GRCh37
NC_000014.7:g.32352221C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000280979.9:c.3589-8138C>G MANE Select ENSP00000280979.4:n.3589-8138C>G
ENST00000280979.8:c.3589-8138C>G ENSP00000280979.4:n.3589-8138C>G
ENST00000557272.1:c.3589-16584C>G ENSP00000451247.1:n.3589-16584C>G
NM_004274.4:c.3589-8138C>G NP_004265.3:n.3589-8138C>G
XM_005268219.3:c.3592-8138C>G XP_005268276.1:n.3592-8138C>G
XM_011537378.1:c.877-8138C>G XP_011535680.1:n.877-8138C>G
XM_011537379.1:c.808-8138C>G XP_011535681.1:n.808-8138C>G
XM_011537380.1:c.808-8138C>G XP_011535682.1:n.808-8138C>G
XM_011537381.1:c.658-8138C>G XP_011535683.1:n.658-8138C>G
XM_011537382.1:c.658-8138C>G XP_011535684.1:n.658-8138C>G
XM_011537383.1:c.574-8138C>G XP_011535685.1:n.574-8138C>G
XM_011537378.3:c.877-8138C>G XP_011535680.1:n.877-8138C>G
XM_011537379.3:c.808-8138C>G XP_011535681.1:n.808-8138C>G
XM_011537383.3:c.574-8138C>G XP_011535685.1:n.574-8138C>G
XM_017021808.2:c.3592-8138C>G XP_016877297.1:n.3592-8138C>G
XM_017021811.2:c.877-8138C>G XP_016877300.1:n.877-8138C>G
XM_024449754.1:c.3592-8138C>G XP_024305522.1:n.3592-8138C>G
XM_024449755.1:c.3592-8138C>G XP_024305523.1:n.3592-8138C>G
XM_024449756.1:c.3592-8138C>G XP_024305524.1:n.3592-8138C>G
XM_024449757.1:c.3592-8138C>G XP_024305525.1:n.3592-8138C>G
NM_004274.5:c.3589-8138C>G MANE Select NP_004265.3:n.3589-8138C>G