Canonical Allele Identifier: CA2251265576
Gene: AKAP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19909257C= , CM000679.2:g.19909257C= GRCh38
NC_000017.10:g.19812570C= , CM000679.1:g.19812570C= GRCh37
NC_000017.9:g.19753162C= NCBI36
NG_011493.1:g.73560G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225737.11:c.1907G= MANE Select ENSP00000225737.6:p.Trp636=
ENST00000225737.10:c.1907G= ENSP00000225737.6:p.Trp636=
ENST00000395536.7:c.1733G= ENSP00000378907.3:p.Trp578=
ENST00000578898.1:c.334G=
ENST00000583951.1:c.218G= ENSP00000463398.1:p.Trp73=
NM_007202.3:c.1907G= NP_009133.2:p.Trp636=
XM_006721431.2:c.1835-3025G= XP_006721494.1:n.1835-3025G=
XM_006721432.2:c.1733G= XP_006721495.1:p.Trp578=
XR_933969.1:n.1955G=
XR_933970.1:n.1883-3025G=
NM_001330152.1:c.1733G= NP_001317081.1:p.Trp578=
XR_001752418.2:n.2019G=
XR_933969.3:n.1938G=
NM_007202.4:c.1907G= MANE Select NP_009133.2:p.Trp636=
NM_001330152.2:c.1733G= NP_001317081.1:p.Trp578=