Canonical Allele Identifier: CA498642254

Gene: AKAP10

Linked Data

• MyVariant Identifiers: chr17:g.19812563A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909250A>T , CM000679.2:g.19909250A>T	GRCh38
NC_000017.10:g.19812563A>T , CM000679.1:g.19812563A>T	GRCh37
NC_000017.9:g.19753155A>T	NCBI36
NG_011493.1:g.73567T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225737.11:c.1914T>A MANE Select	ENSP00000225737.6:p.Ile638=
ENST00000225737.10:c.1914T>A	ENSP00000225737.6:p.Ile638=
ENST00000395536.7:c.1740T>A	ENSP00000378907.3:p.Ile580=
ENST00000578898.1:c.341T>A
ENST00000583951.1:c.225T>A	ENSP00000463398.1:p.Ile75=
NM_007202.3:c.1914T>A	NP_009133.2:p.Ile638=
XM_006721431.2:c.1835-3018T>A	XP_006721494.1:n.1835-3018T>A
XM_006721432.2:c.1740T>A	XP_006721495.1:p.Ile580=
XR_933969.1:n.1962T>A
XR_933970.1:n.1883-3018T>A
NM_001330152.1:c.1740T>A	NP_001317081.1:p.Ile580=
XR_001752418.2:n.2026T>A
XR_933969.3:n.1945T>A
NM_007202.4:c.1914T>A MANE Select	NP_009133.2:p.Ile638=
NM_001330152.2:c.1740T>A	NP_001317081.1:p.Ile580=