Canonical Allele Identifier: CA2251265566

Gene: AKAP10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909231_19909235delinsCACTG , CM000679.2:g.19909231_19909235delinsCACTG	GRCh38
NC_000017.10:g.19812544_19812548delinsCACTG , CM000679.1:g.19812544_19812548delinsCACTG	GRCh37
NC_000017.9:g.19753136_19753140delinsCACTG	NCBI36
NG_011493.1:g.73582_73586delinsCAGTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000225737.11:c.1929_1933delinsCAGTG MANE Select	ENSP00000225737.6:p.Val643=
ENST00000225737.10:c.1929_1933delinsCAGTG	ENSP00000225737.6:p.Val643=
ENST00000395536.7:c.1755_1759delinsCAGTG	ENSP00000378907.3:p.Val585=
ENST00000578898.1:c.356_360delinsCAGTG
NM_007202.3:c.1929_1933delinsCAGTG	NP_009133.2:p.Val643=
XM_006721431.2:c.1835-3003_1835-2999delinsCAGTG	XP_006721494.1:n.1835-3003_1835-2999delinsCAGTG
XM_006721432.2:c.1755_1759delinsCAGTG	XP_006721495.1:p.Val585=
XR_933969.1:n.1977_1981delinsCAGTG
XR_933970.1:n.1883-3003_1883-2999delinsCAGTG
NM_001330152.1:c.1755_1759delinsCAGTG	NP_001317081.1:p.Val585=
XR_001752418.2:n.2041_2045delinsCAGTG
XR_933969.3:n.1960_1964delinsCAGTG
NM_007202.4:c.1929_1933delinsCAGTG MANE Select	NP_009133.2:p.Val643=
NM_001330152.2:c.1755_1759delinsCAGTG	NP_001317081.1:p.Val585=