Canonical Allele Identifier: CA8445640

Gene: AKAP10

Linked Data

• dbSNP Id: rs138663265
• ExAC: 17:19812512 C / T
• gnomAD v2: 17-19812512-C-T
• gnomAD v3: 17-19909199-C-T
• gnomAD v4: 17-19909199-C-T
• MyVariant Identifiers: chr17:g.19812512C>T (hg19) ; chr17:g.19909199C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909199C>T , CM000679.2:g.19909199C>T	GRCh38
NC_000017.10:g.19812512C>T , CM000679.1:g.19812512C>T	GRCh37
NC_000017.9:g.19753104C>T	NCBI36
NG_011493.1:g.73618G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225737.11:c.1965G>A MANE Select	ENSP00000225737.6:p.Pro655=
ENST00000225737.10:c.1965G>A	ENSP00000225737.6:p.Pro655=
ENST00000395536.7:c.1791G>A	ENSP00000378907.3:p.Pro597=
ENST00000578898.1:c.392G>A
NM_007202.3:c.1965G>A	NP_009133.2:p.Pro655=
XM_006721431.2:c.1835-2967G>A	XP_006721494.1:n.1835-2967G>A
XM_006721432.2:c.1791G>A	XP_006721495.1:p.Pro597=
XR_933969.1:n.2013G>A
XR_933970.1:n.1883-2967G>A
NM_001330152.1:c.1791G>A	NP_001317081.1:p.Pro597=
XR_001752418.2:n.2077G>A
XR_933969.3:n.1996G>A
NM_007202.4:c.1965G>A MANE Select	NP_009133.2:p.Pro655=
NM_001330152.2:c.1791G>A	NP_001317081.1:p.Pro597=