Canonical Allele Identifier: CA2251265572
Gene: AKAP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19909244T= , CM000679.2:g.19909244T= GRCh38
NC_000017.10:g.19812557T= , CM000679.1:g.19812557T= GRCh37
NC_000017.9:g.19753149T= NCBI36
NG_011493.1:g.73573A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225737.11:c.1920A= MANE Select ENSP00000225737.6:p.Lys640=
ENST00000225737.10:c.1920A= ENSP00000225737.6:p.Lys640=
ENST00000395536.7:c.1746A= ENSP00000378907.3:p.Lys582=
ENST00000578898.1:c.347A=
ENST00000583951.1:c.231A= ENSP00000463398.1:p.Lys77=
NM_007202.3:c.1920A= NP_009133.2:p.Lys640=
XM_006721431.2:c.1835-3012A= XP_006721494.1:n.1835-3012A=
XM_006721432.2:c.1746A= XP_006721495.1:p.Lys582=
XR_933969.1:n.1968A=
XR_933970.1:n.1883-3012A=
NM_001330152.1:c.1746A= NP_001317081.1:p.Lys582=
XR_001752418.2:n.2032A=
XR_933969.3:n.1951A=
NM_007202.4:c.1920A= MANE Select NP_009133.2:p.Lys640=
NM_001330152.2:c.1746A= NP_001317081.1:p.Lys582=