Canonical Allele Identifier: CA2576200378

Gene: AKAP10

Linked Data

• gnomAD v4: 17-19909317-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909317T>C , CM000679.2:g.19909317T>C	GRCh38
NC_000017.10:g.19812630T>C , CM000679.1:g.19812630T>C	GRCh37
NC_000017.9:g.19753222T>C	NCBI36
NG_011493.1:g.73500A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225737.11:c.1888-41A>G MANE Select	ENSP00000225737.6:n.1888-41A>G
ENST00000225737.10:c.1888-41A>G	ENSP00000225737.6:n.1888-41A>G
ENST00000395536.7:c.1714-41A>G	ENSP00000378907.3:n.1714-41A>G
ENST00000578898.1:c.315-41A>G
ENST00000583951.1:c.199-41A>G	ENSP00000463398.1:n.199-41A>G
NM_007202.3:c.1888-41A>G	NP_009133.2:n.1888-41A>G
XM_006721431.2:c.1835-3085A>G	XP_006721494.1:n.1835-3085A>G
XM_006721432.2:c.1714-41A>G	XP_006721495.1:n.1714-41A>G
XR_933969.1:n.1936-41A>G
XR_933970.1:n.1883-3085A>G
NM_001330152.1:c.1714-41A>G	NP_001317081.1:n.1714-41A>G
XR_001752418.2:n.2000-41A>G
XR_933969.3:n.1919-41A>G
NM_007202.4:c.1888-41A>G MANE Select	NP_009133.2:n.1888-41A>G
NM_001330152.2:c.1714-41A>G	NP_001317081.1:n.1714-41A>G