Canonical Allele Identifier: CA726841989

Gene: AKAP10

Linked Data

• dbSNP Id: rs1317457889
• MyVariant Identifiers: chr17:g.19812603del (hg19) ; chr17:g.19909290del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909292del , CM000679.2:g.19909292del	GRCh38
NC_000017.10:g.19812605del , CM000679.1:g.19812605del	GRCh37
NC_000017.9:g.19753197del	NCBI36
NG_011493.1:g.73527del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225737.11:c.1888-14del MANE Select	ENSP00000225737.6:n.1888-14del
ENST00000225737.10:c.1888-14del	ENSP00000225737.6:n.1888-14del
ENST00000395536.7:c.1714-14del	ENSP00000378907.3:n.1714-14del
ENST00000578898.1:c.315-14del
ENST00000583951.1:c.199-14del	ENSP00000463398.1:n.199-14del
NM_007202.3:c.1888-14del	NP_009133.2:n.1888-14del
XM_006721431.2:c.1835-3058del	XP_006721494.1:n.1835-3058del
XM_006721432.2:c.1714-14del	XP_006721495.1:n.1714-14del
XR_933969.1:n.1936-14del
XR_933970.1:n.1883-3058del
NM_001330152.1:c.1714-14del	NP_001317081.1:n.1714-14del
XR_001752418.2:n.2000-14del
XR_933969.3:n.1919-14del
NM_007202.4:c.1888-14del MANE Select	NP_009133.2:n.1888-14del
NM_001330152.2:c.1714-14del	NP_001317081.1:n.1714-14del