Canonical Allele Identifier: CA2251265574
Gene: AKAP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19909251A= , CM000679.2:g.19909251A= GRCh38
NC_000017.10:g.19812564A= , CM000679.1:g.19812564A= GRCh37
NC_000017.9:g.19753156A= NCBI36
NG_011493.1:g.73566T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225737.11:c.1913T= MANE Select ENSP00000225737.6:p.Ile638=
ENST00000225737.10:c.1913T= ENSP00000225737.6:p.Ile638=
ENST00000395536.7:c.1739T= ENSP00000378907.3:p.Ile580=
ENST00000578898.1:c.340T=
ENST00000583951.1:c.224T= ENSP00000463398.1:p.Ile75=
NM_007202.3:c.1913T= NP_009133.2:p.Ile638=
XM_006721431.2:c.1835-3019T= XP_006721494.1:n.1835-3019T=
XM_006721432.2:c.1739T= XP_006721495.1:p.Ile580=
XR_933969.1:n.1961T=
XR_933970.1:n.1883-3019T=
NM_001330152.1:c.1739T= NP_001317081.1:p.Ile580=
XR_001752418.2:n.2025T=
XR_933969.3:n.1944T=
NM_007202.4:c.1913T= MANE Select NP_009133.2:p.Ile638=
NM_001330152.2:c.1739T= NP_001317081.1:p.Ile580=