Canonical Allele Identifier: CA2636625635

Gene: AKAP10

Linked Data

• gnomAD v4: 17-19909060-TAAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909064_19909066del , CM000679.2:g.19909064_19909066del	GRCh38
NC_000017.10:g.19812377_19812379del , CM000679.1:g.19812377_19812379del	GRCh37
NC_000017.9:g.19752969_19752971del	NCBI36
NG_011493.1:g.73754_73756del

Transcript Alleles

HGVS	Amino-acid change
ENST00000225737.11:c.1983+118_1983+120del MANE Select	ENSP00000225737.6:n.1983+118_1983+120del
ENST00000225737.10:c.1983+118_1983+120del	ENSP00000225737.6:n.1983+118_1983+120del
ENST00000395536.7:c.1809+118_1809+120del	ENSP00000378907.3:n.1809+118_1809+120del
ENST00000578898.1:c.410+118_410+120del
NM_007202.3:c.1983+118_1983+120del	NP_009133.2:n.1983+118_1983+120del
XM_006721431.2:c.1835-2831_1835-2829del	XP_006721494.1:n.1835-2831_1835-2829del
XM_006721432.2:c.1809+118_1809+120del	XP_006721495.1:n.1809+118_1809+120del
XR_933969.1:n.2031+118_2031+120del
XR_933970.1:n.1883-2831_1883-2829del
NM_001330152.1:c.1809+118_1809+120del	NP_001317081.1:n.1809+118_1809+120del
XR_001752418.2:n.2095+118_2095+120del
XR_933969.3:n.2014+118_2014+120del
NM_007202.4:c.1983+118_1983+120del MANE Select	NP_009133.2:n.1983+118_1983+120del
NM_001330152.2:c.1809+118_1809+120del	NP_001317081.1:n.1809+118_1809+120del