Canonical Allele Identifier: CA2251265539

Gene: AKAP10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909166_19909167delinsCG , CM000679.2:g.19909166_19909167delinsCG	GRCh38
NC_000017.10:g.19812479_19812480delinsCG , CM000679.1:g.19812479_19812480delinsCG	GRCh37
NC_000017.9:g.19753071_19753072delinsCG	NCBI36
NG_011493.1:g.73650_73651delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225737.11:c.1983+14_1983+15delinsCG MANE Select	ENSP00000225737.6:n.1983+14_1983+15delinsCG
ENST00000225737.10:c.1983+14_1983+15delinsCG	ENSP00000225737.6:n.1983+14_1983+15delinsCG
ENST00000395536.7:c.1809+14_1809+15delinsCG	ENSP00000378907.3:n.1809+14_1809+15delinsCG
ENST00000578898.1:c.410+14_410+15delinsCG
NM_007202.3:c.1983+14_1983+15delinsCG	NP_009133.2:n.1983+14_1983+15delinsCG
XM_006721431.2:c.1835-2935_1835-2934delinsCG	XP_006721494.1:n.1835-2935_1835-2934delinsCG
XM_006721432.2:c.1809+14_1809+15delinsCG	XP_006721495.1:n.1809+14_1809+15delinsCG
XR_933969.1:n.2031+14_2031+15delinsCG
XR_933970.1:n.1883-2935_1883-2934delinsCG
NM_001330152.1:c.1809+14_1809+15delinsCG	NP_001317081.1:n.1809+14_1809+15delinsCG
XR_001752418.2:n.2095+14_2095+15delinsCG
XR_933969.3:n.2014+14_2014+15delinsCG
NM_007202.4:c.1983+14_1983+15delinsCG MANE Select	NP_009133.2:n.1983+14_1983+15delinsCG
NM_001330152.2:c.1809+14_1809+15delinsCG	NP_001317081.1:n.1809+14_1809+15delinsCG