Canonical Allele Identifier: CA625113209

Gene: AKAP10

Linked Data

• dbSNP Id: rs1213531400
• gnomAD v2: 17-19812457-A-G
• gnomAD v3: 17-19909144-A-G
• gnomAD v4: 17-19909144-A-G
• MyVariant Identifiers: chr17:g.19812457A>G (hg19) ; chr17:g.19909144A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909144A>G , CM000679.2:g.19909144A>G	GRCh38
NC_000017.10:g.19812457A>G , CM000679.1:g.19812457A>G	GRCh37
NC_000017.9:g.19753049A>G	NCBI36
NG_011493.1:g.73673T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000225737.11:c.1983+37T>C MANE Select	ENSP00000225737.6:n.1983+37T>C
ENST00000225737.10:c.1983+37T>C	ENSP00000225737.6:n.1983+37T>C
ENST00000395536.7:c.1809+37T>C	ENSP00000378907.3:n.1809+37T>C
ENST00000578898.1:c.410+37T>C
NM_007202.3:c.1983+37T>C	NP_009133.2:n.1983+37T>C
XM_006721431.2:c.1835-2912T>C	XP_006721494.1:n.1835-2912T>C
XM_006721432.2:c.1809+37T>C	XP_006721495.1:n.1809+37T>C
XR_933969.1:n.2031+37T>C
XR_933970.1:n.1883-2912T>C
NM_001330152.1:c.1809+37T>C	NP_001317081.1:n.1809+37T>C
XR_001752418.2:n.2095+37T>C
XR_933969.3:n.2014+37T>C
NM_007202.4:c.1983+37T>C MANE Select	NP_009133.2:n.1983+37T>C
NM_001330152.2:c.1809+37T>C	NP_001317081.1:n.1809+37T>C