Canonical Allele Identifier: CA2251265564
Gene: AKAP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19909229G= , CM000679.2:g.19909229G= GRCh38
NC_000017.10:g.19812542G= , CM000679.1:g.19812542G= GRCh37
NC_000017.9:g.19753134G= NCBI36
NG_011493.1:g.73588C=

Transcript Alleles

HGVS Amino-acid change
ENST00000225737.11:c.1935C= MANE Select ENSP00000225737.6:p.Asp645=
ENST00000225737.10:c.1935C= ENSP00000225737.6:p.Asp645=
ENST00000395536.7:c.1761C= ENSP00000378907.3:p.Asp587=
ENST00000578898.1:c.362C=
NM_007202.3:c.1935C= NP_009133.2:p.Asp645=
XM_006721431.2:c.1835-2997C= XP_006721494.1:n.1835-2997C=
XM_006721432.2:c.1761C= XP_006721495.1:p.Asp587=
XR_933969.1:n.1983C=
XR_933970.1:n.1883-2997C=
NM_001330152.1:c.1761C= NP_001317081.1:p.Asp587=
XR_001752418.2:n.2047C=
XR_933969.3:n.1966C=
NM_007202.4:c.1935C= MANE Select NP_009133.2:p.Asp645=
NM_001330152.2:c.1761C= NP_001317081.1:p.Asp587=