Canonical Allele Identifier: CA288594057

Gene: AKAP10

Linked Data

• dbSNP Id: rs796096871

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909228_19909229delinsCA , CM000679.2:g.19909228_19909229delinsCA	GRCh38
NC_000017.10:g.19812541_19812542delinsCA , CM000679.1:g.19812541_19812542delinsCA	GRCh37
NC_000017.9:g.19753133_19753134delinsCA	NCBI36
NG_011493.1:g.73588_73589delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225737.11:c.1935_1936delinsTG MANE Select	ENSP00000225737.6:p.Ile646Val
ENST00000225737.10:c.1935_1936delinsTG	ENSP00000225737.6:p.Ile646Val
ENST00000395536.7:c.1761_1762delinsTG	ENSP00000378907.3:p.Ile588Val
ENST00000578898.1:c.362_363delinsTG
NM_007202.3:c.1935_1936delinsTG	NP_009133.2:p.Ile646Val
XM_006721431.2:c.1835-2997_1835-2996delinsTG	XP_006721494.1:n.1835-2997_1835-2996delinsTG
XM_006721432.2:c.1761_1762delinsTG	XP_006721495.1:p.Ile588Val
XR_933969.1:n.1983_1984delinsTG
XR_933970.1:n.1883-2997_1883-2996delinsTG
NM_001330152.1:c.1761_1762delinsTG	NP_001317081.1:p.Ile588Val
XR_001752418.2:n.2047_2048delinsTG
XR_933969.3:n.1966_1967delinsTG
NM_007202.4:c.1935_1936delinsTG MANE Select	NP_009133.2:p.Ile646Val
NM_001330152.2:c.1761_1762delinsTG	NP_001317081.1:p.Ile588Val