Canonical Allele Identifier: CA288594008

Gene: AKAP10

Linked Data

• dbSNP Id: rs934223560
• gnomAD v3: 17-19909029-T-C
• gnomAD v4: 17-19909029-T-C
• MyVariant Identifiers: chr17:g.19812342T>C (hg19) ; chr17:g.19909029T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909029T>C , CM000679.2:g.19909029T>C	GRCh38
NC_000017.10:g.19812342T>C , CM000679.1:g.19812342T>C	GRCh37
NC_000017.9:g.19752934T>C	NCBI36
NG_011493.1:g.73788A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000225737.11:c.1983+152A>G MANE Select	ENSP00000225737.6:n.1983+152A>G
ENST00000225737.10:c.1983+152A>G	ENSP00000225737.6:n.1983+152A>G
ENST00000395536.7:c.1809+152A>G	ENSP00000378907.3:n.1809+152A>G
ENST00000578898.1:c.410+152A>G
NM_007202.3:c.1983+152A>G	NP_009133.2:n.1983+152A>G
XM_006721431.2:c.1835-2797A>G	XP_006721494.1:n.1835-2797A>G
XM_006721432.2:c.1809+152A>G	XP_006721495.1:n.1809+152A>G
XR_933969.1:n.2031+152A>G
XR_933970.1:n.1883-2797A>G
NM_001330152.1:c.1809+152A>G	NP_001317081.1:n.1809+152A>G
XR_001752418.2:n.2095+152A>G
XR_933969.3:n.2014+152A>G
NM_007202.4:c.1983+152A>G MANE Select	NP_009133.2:n.1983+152A>G
NM_001330152.2:c.1809+152A>G	NP_001317081.1:n.1809+152A>G