Canonical Allele Identifier: CA498642225

Gene: AKAP10

Linked Data

• MyVariant Identifiers: chr17:g.19812500A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909187A>C , CM000679.2:g.19909187A>C	GRCh38
NC_000017.10:g.19812500A>C , CM000679.1:g.19812500A>C	GRCh37
NC_000017.9:g.19753092A>C	NCBI36
NG_011493.1:g.73630T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000225737.11:c.1977T>G MANE Select	ENSP00000225737.6:p.Ser659=
ENST00000225737.10:c.1977T>G	ENSP00000225737.6:p.Ser659=
ENST00000395536.7:c.1803T>G	ENSP00000378907.3:p.Ser601=
ENST00000578898.1:c.404T>G
NM_007202.3:c.1977T>G	NP_009133.2:p.Ser659=
XM_006721431.2:c.1835-2955T>G	XP_006721494.1:n.1835-2955T>G
XM_006721432.2:c.1803T>G	XP_006721495.1:p.Ser601=
XR_933969.1:n.2025T>G
XR_933970.1:n.1883-2955T>G
NM_001330152.1:c.1803T>G	NP_001317081.1:p.Ser601=
XR_001752418.2:n.2089T>G
XR_933969.3:n.2008T>G
NM_007202.4:c.1977T>G MANE Select	NP_009133.2:p.Ser659=
NM_001330152.2:c.1803T>G	NP_001317081.1:p.Ser601=