Canonical Allele Identifier: CA2251265529
Gene: AKAP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19909131C= , CM000679.2:g.19909131C= GRCh38
NC_000017.10:g.19812444C= , CM000679.1:g.19812444C= GRCh37
NC_000017.9:g.19753036C= NCBI36
NG_011493.1:g.73686G=

Transcript Alleles

HGVS Amino-acid change
ENST00000225737.11:c.1983+50G= MANE Select ENSP00000225737.6:n.1983+50G=
ENST00000225737.10:c.1983+50G= ENSP00000225737.6:n.1983+50G=
ENST00000395536.7:c.1809+50G= ENSP00000378907.3:n.1809+50G=
ENST00000578898.1:c.410+50G=
NM_007202.3:c.1983+50G= NP_009133.2:n.1983+50G=
XM_006721431.2:c.1835-2899G= XP_006721494.1:n.1835-2899G=
XM_006721432.2:c.1809+50G= XP_006721495.1:n.1809+50G=
XR_933969.1:n.2031+50G=
XR_933970.1:n.1883-2899G=
NM_001330152.1:c.1809+50G= NP_001317081.1:n.1809+50G=
XR_001752418.2:n.2095+50G=
XR_933969.3:n.2014+50G=
NM_007202.4:c.1983+50G= MANE Select NP_009133.2:n.1983+50G=
NM_001330152.2:c.1809+50G= NP_001317081.1:n.1809+50G=