Canonical Allele Identifier: CA398726137

Gene: AKAP10

Linked Data

• dbSNP Id: rs1485149600
• gnomAD v2: 17-19812545-A-T
• gnomAD v3: 17-19909232-A-T
• gnomAD v4: 17-19909232-A-T
• MyVariant Identifiers: chr17:g.19812545A>T (hg19) ; chr17:g.19909232A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909232A>T , CM000679.2:g.19909232A>T	GRCh38
NC_000017.10:g.19812545A>T , CM000679.1:g.19812545A>T	GRCh37
NC_000017.9:g.19753137A>T	NCBI36
NG_011493.1:g.73585T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000225737.11:c.1932T>A MANE Select	ENSP00000225737.6:p.Ser644Arg
ENST00000225737.10:c.1932T>A	ENSP00000225737.6:p.Ser644Arg
ENST00000395536.7:c.1758T>A	ENSP00000378907.3:p.Ser586Arg
ENST00000578898.1:c.359T>A
NM_007202.3:c.1932T>A	NP_009133.2:p.Ser644Arg
XM_006721431.2:c.1835-3000T>A	XP_006721494.1:n.1835-3000T>A
XM_006721432.2:c.1758T>A	XP_006721495.1:p.Ser586Arg
XR_933969.1:n.1980T>A
XR_933970.1:n.1883-3000T>A
NM_001330152.1:c.1758T>A	NP_001317081.1:p.Ser586Arg
XR_001752418.2:n.2044T>A
XR_933969.3:n.1963T>A
NM_007202.4:c.1932T>A MANE Select	NP_009133.2:p.Ser644Arg
NM_001330152.2:c.1758T>A	NP_001317081.1:p.Ser586Arg