Canonical Allele Identifier: CA498642243

Gene: AKAP10

Linked Data

• MyVariant Identifiers: chr17:g.19812545A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909232A>G , CM000679.2:g.19909232A>G	GRCh38
NC_000017.10:g.19812545A>G , CM000679.1:g.19812545A>G	GRCh37
NC_000017.9:g.19753137A>G	NCBI36
NG_011493.1:g.73585T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000225737.11:c.1932T>C MANE Select	ENSP00000225737.6:p.Ser644=
ENST00000225737.10:c.1932T>C	ENSP00000225737.6:p.Ser644=
ENST00000395536.7:c.1758T>C	ENSP00000378907.3:p.Ser586=
ENST00000578898.1:c.359T>C
NM_007202.3:c.1932T>C	NP_009133.2:p.Ser644=
XM_006721431.2:c.1835-3000T>C	XP_006721494.1:n.1835-3000T>C
XM_006721432.2:c.1758T>C	XP_006721495.1:p.Ser586=
XR_933969.1:n.1980T>C
XR_933970.1:n.1883-3000T>C
NM_001330152.1:c.1758T>C	NP_001317081.1:p.Ser586=
XR_001752418.2:n.2044T>C
XR_933969.3:n.1963T>C
NM_007202.4:c.1932T>C MANE Select	NP_009133.2:p.Ser644=
NM_001330152.2:c.1758T>C	NP_001317081.1:p.Ser586=