Canonical Allele Identifier: CA398726151

Gene: AKAP10

Linked Data

• MyVariant Identifiers: chr17:g.19812552A>C (hg19) ; chr17:g.19909239A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909239A>C , CM000679.2:g.19909239A>C	GRCh38
NC_000017.10:g.19812552A>C , CM000679.1:g.19812552A>C	GRCh37
NC_000017.9:g.19753144A>C	NCBI36
NG_011493.1:g.73578T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000225737.11:c.1925T>G MANE Select	ENSP00000225737.6:p.Ile642Arg
ENST00000225737.10:c.1925T>G	ENSP00000225737.6:p.Ile642Arg
ENST00000395536.7:c.1751T>G	ENSP00000378907.3:p.Ile584Arg
ENST00000578898.1:c.352T>G
ENST00000583951.1:c.236T>G
NM_007202.3:c.1925T>G	NP_009133.2:p.Ile642Arg
XM_006721431.2:c.1835-3007T>G	XP_006721494.1:n.1835-3007T>G
XM_006721432.2:c.1751T>G	XP_006721495.1:p.Ile584Arg
XR_933969.1:n.1973T>G
XR_933970.1:n.1883-3007T>G
NM_001330152.1:c.1751T>G	NP_001317081.1:p.Ile584Arg
XR_001752418.2:n.2037T>G
XR_933969.3:n.1956T>G
NM_007202.4:c.1925T>G MANE Select	NP_009133.2:p.Ile642Arg
NM_001330152.2:c.1751T>G	NP_001317081.1:p.Ile584Arg