Canonical Allele Identifier: CA8445655

Gene: AKAP10

Linked Data

• dbSNP Id: rs762344054
• ExAC: 17:19812628 A / C
• gnomAD v2: 17-19812628-A-C
• gnomAD v4: 17-19909315-A-C
• MyVariant Identifiers: chr17:g.19812628A>C (hg19) ; chr17:g.19909315A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909315A>C , CM000679.2:g.19909315A>C	GRCh38
NC_000017.10:g.19812628A>C , CM000679.1:g.19812628A>C	GRCh37
NC_000017.9:g.19753220A>C	NCBI36
NG_011493.1:g.73502T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225737.11:c.1888-39T>G MANE Select	ENSP00000225737.6:n.1888-39T>G
ENST00000225737.10:c.1888-39T>G	ENSP00000225737.6:n.1888-39T>G
ENST00000395536.7:c.1714-39T>G	ENSP00000378907.3:n.1714-39T>G
ENST00000578898.1:c.315-39T>G
ENST00000583951.1:c.199-39T>G	ENSP00000463398.1:n.199-39T>G
NM_007202.3:c.1888-39T>G	NP_009133.2:n.1888-39T>G
XM_006721431.2:c.1835-3083T>G	XP_006721494.1:n.1835-3083T>G
XM_006721432.2:c.1714-39T>G	XP_006721495.1:n.1714-39T>G
XR_933969.1:n.1936-39T>G
XR_933970.1:n.1883-3083T>G
NM_001330152.1:c.1714-39T>G	NP_001317081.1:n.1714-39T>G
XR_001752418.2:n.2000-39T>G
XR_933969.3:n.1919-39T>G
NM_007202.4:c.1888-39T>G MANE Select	NP_009133.2:n.1888-39T>G
NM_001330152.2:c.1714-39T>G	NP_001317081.1:n.1714-39T>G