Canonical Allele Identifier: CA398726177

Gene: AKAP10

Linked Data

• MyVariant Identifiers: chr17:g.19812561G>T (hg19) ; chr17:g.19909248G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909248G>T , CM000679.2:g.19909248G>T	GRCh38
NC_000017.10:g.19812561G>T , CM000679.1:g.19812561G>T	GRCh37
NC_000017.9:g.19753153G>T	NCBI36
NG_011493.1:g.73569C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225737.11:c.1916C>A MANE Select	ENSP00000225737.6:p.Ala639Asp
ENST00000225737.10:c.1916C>A	ENSP00000225737.6:p.Ala639Asp
ENST00000395536.7:c.1742C>A	ENSP00000378907.3:p.Ala581Asp
ENST00000578898.1:c.343C>A
ENST00000583951.1:c.227C>A	ENSP00000463398.1:p.Ala76Asp
NM_007202.3:c.1916C>A	NP_009133.2:p.Ala639Asp
XM_006721431.2:c.1835-3016C>A	XP_006721494.1:n.1835-3016C>A
XM_006721432.2:c.1742C>A	XP_006721495.1:p.Ala581Asp
XR_933969.1:n.1964C>A
XR_933970.1:n.1883-3016C>A
NM_001330152.1:c.1742C>A	NP_001317081.1:p.Ala581Asp
XR_001752418.2:n.2028C>A
XR_933969.3:n.1947C>A
NM_007202.4:c.1916C>A MANE Select	NP_009133.2:p.Ala639Asp
NM_001330152.2:c.1742C>A	NP_001317081.1:p.Ala581Asp