Canonical Allele Identifier: CA2251265567
Gene: AKAP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19909232A= , CM000679.2:g.19909232A= GRCh38
NC_000017.10:g.19812545A= , CM000679.1:g.19812545A= GRCh37
NC_000017.9:g.19753137A= NCBI36
NG_011493.1:g.73585T=

Transcript Alleles

HGVS Amino-acid change
ENST00000225737.11:c.1932T= MANE Select ENSP00000225737.6:p.Ser644=
ENST00000225737.10:c.1932T= ENSP00000225737.6:p.Ser644=
ENST00000395536.7:c.1758T= ENSP00000378907.3:p.Ser586=
ENST00000578898.1:c.359T=
NM_007202.3:c.1932T= NP_009133.2:p.Ser644=
XM_006721431.2:c.1835-3000T= XP_006721494.1:n.1835-3000T=
XM_006721432.2:c.1758T= XP_006721495.1:p.Ser586=
XR_933969.1:n.1980T=
XR_933970.1:n.1883-3000T=
NM_001330152.1:c.1758T= NP_001317081.1:p.Ser586=
XR_001752418.2:n.2044T=
XR_933969.3:n.1963T=
NM_007202.4:c.1932T= MANE Select NP_009133.2:p.Ser644=
NM_001330152.2:c.1758T= NP_001317081.1:p.Ser586=