Canonical Allele Identifier: CA8445652

Gene: AKAP10

Linked Data

• dbSNP Id: rs749586498
• ExAC: 17:19812617 A / G
• gnomAD v2: 17-19812617-A-G
• gnomAD v4: 17-19909304-A-G
• MyVariant Identifiers: chr17:g.19812617A>G (hg19) ; chr17:g.19909304A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909304A>G , CM000679.2:g.19909304A>G	GRCh38
NC_000017.10:g.19812617A>G , CM000679.1:g.19812617A>G	GRCh37
NC_000017.9:g.19753209A>G	NCBI36
NG_011493.1:g.73513T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225737.11:c.1888-28T>C MANE Select	ENSP00000225737.6:n.1888-28T>C
ENST00000225737.10:c.1888-28T>C	ENSP00000225737.6:n.1888-28T>C
ENST00000395536.7:c.1714-28T>C	ENSP00000378907.3:n.1714-28T>C
ENST00000578898.1:c.315-28T>C
ENST00000583951.1:c.199-28T>C	ENSP00000463398.1:n.199-28T>C
NM_007202.3:c.1888-28T>C	NP_009133.2:n.1888-28T>C
XM_006721431.2:c.1835-3072T>C	XP_006721494.1:n.1835-3072T>C
XM_006721432.2:c.1714-28T>C	XP_006721495.1:n.1714-28T>C
XR_933969.1:n.1936-28T>C
XR_933970.1:n.1883-3072T>C
NM_001330152.1:c.1714-28T>C	NP_001317081.1:n.1714-28T>C
XR_001752418.2:n.2000-28T>C
XR_933969.3:n.1919-28T>C
NM_007202.4:c.1888-28T>C MANE Select	NP_009133.2:n.1888-28T>C
NM_001330152.2:c.1714-28T>C	NP_001317081.1:n.1714-28T>C