Canonical Allele Identifier: CA2251265569

Gene: AKAP10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909234T= , CM000679.2:g.19909234T=	GRCh38
NC_000017.10:g.19812547T= , CM000679.1:g.19812547T=	GRCh37
NC_000017.9:g.19753139T=	NCBI36
NG_011493.1:g.73583A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000225737.11:c.1930A= MANE Select	ENSP00000225737.6:p.Ser644=
ENST00000225737.10:c.1930A=	ENSP00000225737.6:p.Ser644=
ENST00000395536.7:c.1756A=	ENSP00000378907.3:p.Ser586=
ENST00000578898.1:c.357A=
NM_007202.3:c.1930A=	NP_009133.2:p.Ser644=
XM_006721431.2:c.1835-3002A=	XP_006721494.1:n.1835-3002A=
XM_006721432.2:c.1756A=	XP_006721495.1:p.Ser586=
XR_933969.1:n.1978A=
XR_933970.1:n.1883-3002A=
NM_001330152.1:c.1756A=	NP_001317081.1:p.Ser586=
XR_001752418.2:n.2042A=
XR_933969.3:n.1961A=
NM_007202.4:c.1930A= MANE Select	NP_009133.2:p.Ser644=
NM_001330152.2:c.1756A=	NP_001317081.1:p.Ser586=