Canonical Allele Identifier: CA2251265486
Gene: AKAP10 HGNC NCBI

Linked Data

dbSNP Id: rs2042662244

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19909036del , CM000679.2:g.19909036del GRCh38
NC_000017.10:g.19812349del , CM000679.1:g.19812349del GRCh37
NC_000017.9:g.19752941del NCBI36
NG_011493.1:g.73783del

Transcript Alleles

HGVS Amino-acid change
ENST00000225737.11:c.1983+147del MANE Select ENSP00000225737.6:n.1983+147del
ENST00000225737.10:c.1983+147del ENSP00000225737.6:n.1983+147del
ENST00000395536.7:c.1809+147del ENSP00000378907.3:n.1809+147del
ENST00000578898.1:c.410+147del
NM_007202.3:c.1983+147del NP_009133.2:n.1983+147del
XM_006721431.2:c.1835-2802del XP_006721494.1:n.1835-2802del
XM_006721432.2:c.1809+147del XP_006721495.1:n.1809+147del
XR_933969.1:n.2031+147del
XR_933970.1:n.1883-2802del
NM_001330152.1:c.1809+147del NP_001317081.1:n.1809+147del
XR_001752418.2:n.2095+147del
XR_933969.3:n.2014+147del
NM_007202.4:c.1983+147del MANE Select NP_009133.2:n.1983+147del
NM_001330152.2:c.1809+147del NP_001317081.1:n.1809+147del