Canonical Allele Identifier: CA2251265479

Gene: AKAP10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909029T= , CM000679.2:g.19909029T=	GRCh38
NC_000017.10:g.19812342T= , CM000679.1:g.19812342T=	GRCh37
NC_000017.9:g.19752934T=	NCBI36
NG_011493.1:g.73788A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225737.11:c.1983+152A= MANE Select	ENSP00000225737.6:n.1983+152A=
ENST00000225737.10:c.1983+152A=	ENSP00000225737.6:n.1983+152A=
ENST00000395536.7:c.1809+152A=	ENSP00000378907.3:n.1809+152A=
ENST00000578898.1:c.410+152A=
NM_007202.3:c.1983+152A=	NP_009133.2:n.1983+152A=
XM_006721431.2:c.1835-2797A=	XP_006721494.1:n.1835-2797A=
XM_006721432.2:c.1809+152A=	XP_006721495.1:n.1809+152A=
XR_933969.1:n.2031+152A=
XR_933970.1:n.1883-2797A=
NM_001330152.1:c.1809+152A=	NP_001317081.1:n.1809+152A=
XR_001752418.2:n.2095+152A=
XR_933969.3:n.2014+152A=
NM_007202.4:c.1983+152A= MANE Select	NP_009133.2:n.1983+152A=
NM_001330152.2:c.1809+152A=	NP_001317081.1:n.1809+152A=