Canonical Allele Identifier: CA2591452120

Gene: AKAP10

Linked Data

• gnomAD v3: 17-19909024-T-TTTCATTTAGTTTGTCAATTTTCTAGTTGC
• gnomAD v4: 17-19909024-T-TTTCATTTAGTTTGTCAATTTTCTAGTTGC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909027_19909055dup , CM000679.2:g.19909027_19909055dup	GRCh38
NC_000017.10:g.19812340_19812368dup , CM000679.1:g.19812340_19812368dup	GRCh37
NC_000017.9:g.19752932_19752960dup	NCBI36
NG_011493.1:g.73764_73792dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000225737.11:c.1983+128_1983+156dup MANE Select	ENSP00000225737.6:n.1983+128_1983+156dup
ENST00000225737.10:c.1983+128_1983+156dup	ENSP00000225737.6:n.1983+128_1983+156dup
ENST00000395536.7:c.1809+128_1809+156dup	ENSP00000378907.3:n.1809+128_1809+156dup
ENST00000578898.1:c.410+128_410+156dup
NM_007202.3:c.1983+128_1983+156dup	NP_009133.2:n.1983+128_1983+156dup
XM_006721431.2:c.1835-2821_1835-2793dup	XP_006721494.1:n.1835-2821_1835-2793dup
XM_006721432.2:c.1809+128_1809+156dup	XP_006721495.1:n.1809+128_1809+156dup
XR_933969.1:n.2031+128_2031+156dup
XR_933970.1:n.1883-2821_1883-2793dup
NM_001330152.1:c.1809+128_1809+156dup	NP_001317081.1:n.1809+128_1809+156dup
XR_001752418.2:n.2095+128_2095+156dup
XR_933969.3:n.2014+128_2014+156dup
NM_007202.4:c.1983+128_1983+156dup MANE Select	NP_009133.2:n.1983+128_1983+156dup
NM_001330152.2:c.1809+128_1809+156dup	NP_001317081.1:n.1809+128_1809+156dup