Canonical Allele Identifier: CA498642255

Gene: AKAP10

Linked Data

• MyVariant Identifiers: chr17:g.19812566C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909253C>T , CM000679.2:g.19909253C>T	GRCh38
NC_000017.10:g.19812566C>T , CM000679.1:g.19812566C>T	GRCh37
NC_000017.9:g.19753158C>T	NCBI36
NG_011493.1:g.73564G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225737.11:c.1911G>A MANE Select	ENSP00000225737.6:p.Lys637=
ENST00000225737.10:c.1911G>A	ENSP00000225737.6:p.Lys637=
ENST00000395536.7:c.1737G>A	ENSP00000378907.3:p.Lys579=
ENST00000578898.1:c.338G>A
ENST00000583951.1:c.222G>A	ENSP00000463398.1:p.Lys74=
NM_007202.3:c.1911G>A	NP_009133.2:p.Lys637=
XM_006721431.2:c.1835-3021G>A	XP_006721494.1:n.1835-3021G>A
XM_006721432.2:c.1737G>A	XP_006721495.1:p.Lys579=
XR_933969.1:n.1959G>A
XR_933970.1:n.1883-3021G>A
NM_001330152.1:c.1737G>A	NP_001317081.1:p.Lys579=
XR_001752418.2:n.2023G>A
XR_933969.3:n.1942G>A
NM_007202.4:c.1911G>A MANE Select	NP_009133.2:p.Lys637=
NM_001330152.2:c.1737G>A	NP_001317081.1:p.Lys579=