Canonical Allele Identifier: CA147901151
Gene: AKAP7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131242437G>A , CM000668.2:g.131242437G>A GRCh38
NC_000006.11:g.131563577G>A , CM000668.1:g.131563577G>A GRCh37
NC_000006.10:g.131605270G>A NCBI36
NG_029123.1:g.111752G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000683794.1:c.850+22629G>A ENSP00000506952.1:n.850+22629G>A
ENST00000431975.7:c.850+22629G>A MANE Select ENSP00000405252.2:n.850+22629G>A
ENST00000263050.3:c.58+22629G>A ENSP00000263050.3:n.58+22629G>A
ENST00000431975.6:c.850+22629G>A ENSP00000405252.2:n.850+22629G>A
ENST00000535150.1:n.595+22629G>A
ENST00000537868.5:c.58+22629G>A ENSP00000446022.1:n.58+22629G>A
ENST00000541650.5:c.847+22629G>A ENSP00000441048.1:n.847+22629G>A
NM_016377.3:c.850+22629G>A NP_057461.2:n.850+22629G>A
XM_005267228.1:c.850+22629G>A XP_005267285.1:n.850+22629G>A
XM_005267229.3:c.784+22629G>A XP_005267286.1:n.784+22629G>A
XR_427979.1:n.770+22629G>A
XR_942636.1:n.1027+253G>A
XM_005267229.4:c.784+22629G>A XP_005267286.1:n.784+22629G>A
XM_017011508.1:c.880+22629G>A XP_016866997.1:n.880+22629G>A
XM_017011509.1:c.862+22629G>A XP_016866998.1:n.862+22629G>A
XM_017011510.1:c.493+22629G>A XP_016866999.1:n.493+22629G>A
XM_017011511.2:c.493+22629G>A XP_016867000.1:n.493+22629G>A
XR_002956317.1:n.1087+22629G>A
XR_002956318.1:n.770+22629G>A
XR_942636.2:n.1027+253G>A
NM_016377.4:c.850+22629G>A MANE Select NP_057461.2:n.850+22629G>A
NM_001376570.1:c.850+22629G>A NP_001363499.1:n.850+22629G>A
NR_164832.1:n.1746+22629G>A
NR_164833.1:n.1811+22629G>A
NR_164834.1:n.1351+22629G>A
NM_001387860.1:c.718+22629G>A NP_001374789.1:n.718+22629G>A
NM_001387861.1:c.850+22629G>A NP_001374790.1:n.850+22629G>A
NM_001387863.1:c.784+22629G>A NP_001374792.1:n.784+22629G>A
NR_170716.1:n.1310+22629G>A
NR_170717.1:n.1640+22629G>A
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