Canonical Allele Identifier: CA8445647

Gene: AKAP10

Linked Data

• dbSNP Id: rs200392888
• ExAC: 17:19812542 G / A
• gnomAD v2: 17-19812542-G-A
• gnomAD v3: 17-19909229-G-A
• gnomAD v4: 17-19909229-G-A
• MyVariant Identifiers: chr17:g.19812542G>A (hg19) ; chr17:g.19909229G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909229G>A , CM000679.2:g.19909229G>A	GRCh38
NC_000017.10:g.19812542G>A , CM000679.1:g.19812542G>A	GRCh37
NC_000017.9:g.19753134G>A	NCBI36
NG_011493.1:g.73588C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000225737.11:c.1935C>T MANE Select	ENSP00000225737.6:p.Asp645=
ENST00000225737.10:c.1935C>T	ENSP00000225737.6:p.Asp645=
ENST00000395536.7:c.1761C>T	ENSP00000378907.3:p.Asp587=
ENST00000578898.1:c.362C>T
NM_007202.3:c.1935C>T	NP_009133.2:p.Asp645=
XM_006721431.2:c.1835-2997C>T	XP_006721494.1:n.1835-2997C>T
XM_006721432.2:c.1761C>T	XP_006721495.1:p.Asp587=
XR_933969.1:n.1983C>T
XR_933970.1:n.1883-2997C>T
NM_001330152.1:c.1761C>T	NP_001317081.1:p.Asp587=
XR_001752418.2:n.2047C>T
XR_933969.3:n.1966C>T
NM_007202.4:c.1935C>T MANE Select	NP_009133.2:p.Asp645=
NM_001330152.2:c.1761C>T	NP_001317081.1:p.Asp587=