Canonical Allele Identifier: CA625113202

Gene: AKAP10

Linked Data

• dbSNP Id: rs1362277809
• gnomAD v2: 17-19812374-A-G
• gnomAD v3: 17-19909061-A-G
• gnomAD v4: 17-19909061-A-G
• MyVariant Identifiers: chr17:g.19812374A>G (hg19) ; chr17:g.19909061A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909061A>G , CM000679.2:g.19909061A>G	GRCh38
NC_000017.10:g.19812374A>G , CM000679.1:g.19812374A>G	GRCh37
NC_000017.9:g.19752966A>G	NCBI36
NG_011493.1:g.73756T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225737.11:c.1983+120T>C MANE Select	ENSP00000225737.6:n.1983+120T>C
ENST00000225737.10:c.1983+120T>C	ENSP00000225737.6:n.1983+120T>C
ENST00000395536.7:c.1809+120T>C	ENSP00000378907.3:n.1809+120T>C
ENST00000578898.1:c.410+120T>C
NM_007202.3:c.1983+120T>C	NP_009133.2:n.1983+120T>C
XM_006721431.2:c.1835-2829T>C	XP_006721494.1:n.1835-2829T>C
XM_006721432.2:c.1809+120T>C	XP_006721495.1:n.1809+120T>C
XR_933969.1:n.2031+120T>C
XR_933970.1:n.1883-2829T>C
NM_001330152.1:c.1809+120T>C	NP_001317081.1:n.1809+120T>C
XR_001752418.2:n.2095+120T>C
XR_933969.3:n.2014+120T>C
NM_007202.4:c.1983+120T>C MANE Select	NP_009133.2:n.1983+120T>C
NM_001330152.2:c.1809+120T>C	NP_001317081.1:n.1809+120T>C