Canonical Allele Identifier: CA2251265490

Gene: AKAP10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909041_19909042delinsAT , CM000679.2:g.19909041_19909042delinsAT	GRCh38
NC_000017.10:g.19812354_19812355delinsAT , CM000679.1:g.19812354_19812355delinsAT	GRCh37
NC_000017.9:g.19752946_19752947delinsAT	NCBI36
NG_011493.1:g.73775_73776delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225737.11:c.1983+139_1983+140delinsAT MANE Select	ENSP00000225737.6:n.1983+139_1983+140delinsAT
ENST00000225737.10:c.1983+139_1983+140delinsAT	ENSP00000225737.6:n.1983+139_1983+140delinsAT
ENST00000395536.7:c.1809+139_1809+140delinsAT	ENSP00000378907.3:n.1809+139_1809+140delinsAT
ENST00000578898.1:c.410+139_410+140delinsAT
NM_007202.3:c.1983+139_1983+140delinsAT	NP_009133.2:n.1983+139_1983+140delinsAT
XM_006721431.2:c.1835-2810_1835-2809delinsAT	XP_006721494.1:n.1835-2810_1835-2809delinsAT
XM_006721432.2:c.1809+139_1809+140delinsAT	XP_006721495.1:n.1809+139_1809+140delinsAT
XR_933969.1:n.2031+139_2031+140delinsAT
XR_933970.1:n.1883-2810_1883-2809delinsAT
NM_001330152.1:c.1809+139_1809+140delinsAT	NP_001317081.1:n.1809+139_1809+140delinsAT
XR_001752418.2:n.2095+139_2095+140delinsAT
XR_933969.3:n.2014+139_2014+140delinsAT
NM_007202.4:c.1983+139_1983+140delinsAT MANE Select	NP_009133.2:n.1983+139_1983+140delinsAT
NM_001330152.2:c.1809+139_1809+140delinsAT	NP_001317081.1:n.1809+139_1809+140delinsAT