Canonical Allele Identifier: CA498642251

Gene: AKAP10

Linked Data

• MyVariant Identifiers: chr17:g.19812560A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909247A>T , CM000679.2:g.19909247A>T	GRCh38
NC_000017.10:g.19812560A>T , CM000679.1:g.19812560A>T	GRCh37
NC_000017.9:g.19753152A>T	NCBI36
NG_011493.1:g.73570T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225737.11:c.1917T>A MANE Select	ENSP00000225737.6:p.Ala639=
ENST00000225737.10:c.1917T>A	ENSP00000225737.6:p.Ala639=
ENST00000395536.7:c.1743T>A	ENSP00000378907.3:p.Ala581=
ENST00000578898.1:c.344T>A
ENST00000583951.1:c.228T>A	ENSP00000463398.1:p.Ala76=
NM_007202.3:c.1917T>A	NP_009133.2:p.Ala639=
XM_006721431.2:c.1835-3015T>A	XP_006721494.1:n.1835-3015T>A
XM_006721432.2:c.1743T>A	XP_006721495.1:p.Ala581=
XR_933969.1:n.1965T>A
XR_933970.1:n.1883-3015T>A
NM_001330152.1:c.1743T>A	NP_001317081.1:p.Ala581=
XR_001752418.2:n.2029T>A
XR_933969.3:n.1948T>A
NM_007202.4:c.1917T>A MANE Select	NP_009133.2:p.Ala639=
NM_001330152.2:c.1743T>A	NP_001317081.1:p.Ala581=