Canonical Allele Identifier: CA2251265571
Gene: AKAP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19909243T= , CM000679.2:g.19909243T= GRCh38
NC_000017.10:g.19812556T= , CM000679.1:g.19812556T= GRCh37
NC_000017.9:g.19753148T= NCBI36
NG_011493.1:g.73574A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225737.11:c.1921A= MANE Select ENSP00000225737.6:p.Met641=
ENST00000225737.10:c.1921A= ENSP00000225737.6:p.Met641=
ENST00000395536.7:c.1747A= ENSP00000378907.3:p.Met583=
ENST00000578898.1:c.348A=
ENST00000583951.1:c.232A= ENSP00000463398.1:p.Met78=
NM_007202.3:c.1921A= NP_009133.2:p.Met641=
XM_006721431.2:c.1835-3011A= XP_006721494.1:n.1835-3011A=
XM_006721432.2:c.1747A= XP_006721495.1:p.Met583=
XR_933969.1:n.1969A=
XR_933970.1:n.1883-3011A=
NM_001330152.1:c.1747A= NP_001317081.1:p.Met583=
XR_001752418.2:n.2033A=
XR_933969.3:n.1952A=
NM_007202.4:c.1921A= MANE Select NP_009133.2:p.Met641=
NM_001330152.2:c.1747A= NP_001317081.1:p.Met583=