Canonical Allele Identifier: CA2636625714

Gene: AKAP10

Linked Data

• gnomAD v4: 17-19909335-C-CTGAGT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909335_19909336insTGAGT , CM000679.2:g.19909335_19909336insTGAGT	GRCh38
NC_000017.10:g.19812648_19812649insTGAGT , CM000679.1:g.19812648_19812649insTGAGT	GRCh37
NC_000017.9:g.19753240_19753241insTGAGT	NCBI36
NG_011493.1:g.73481_73482insACTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225737.11:c.1888-60_1888-59insACTCA MANE Select	ENSP00000225737.6:n.1888-60_1888-59insACTCA
ENST00000225737.10:c.1888-60_1888-59insACTCA	ENSP00000225737.6:n.1888-60_1888-59insACTCA
ENST00000395536.7:c.1714-60_1714-59insACTCA	ENSP00000378907.3:n.1714-60_1714-59insACTCA
ENST00000578898.1:c.315-60_315-59insACTCA
ENST00000583951.1:c.199-60_199-59insACTCA	ENSP00000463398.1:n.199-60_199-59insACTCA
NM_007202.3:c.1888-60_1888-59insACTCA	NP_009133.2:n.1888-60_1888-59insACTCA
XM_006721431.2:c.1835-3104_1835-3103insACTCA	XP_006721494.1:n.1835-3104_1835-3103insACTCA
XM_006721432.2:c.1714-60_1714-59insACTCA	XP_006721495.1:n.1714-60_1714-59insACTCA
XR_933969.1:n.1936-60_1936-59insACTCA
XR_933970.1:n.1883-3104_1883-3103insACTCA
NM_001330152.1:c.1714-60_1714-59insACTCA	NP_001317081.1:n.1714-60_1714-59insACTCA
XR_001752418.2:n.2000-60_2000-59insACTCA
XR_933969.3:n.1919-60_1919-59insACTCA
NM_007202.4:c.1888-60_1888-59insACTCA MANE Select	NP_009133.2:n.1888-60_1888-59insACTCA
NM_001330152.2:c.1714-60_1714-59insACTCA	NP_001317081.1:n.1714-60_1714-59insACTCA