Canonical Allele Identifier: CA498642261

Gene: AKAP10

Linked Data

• MyVariant Identifiers: chr17:g.19812575T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909262T>A , CM000679.2:g.19909262T>A	GRCh38
NC_000017.10:g.19812575T>A , CM000679.1:g.19812575T>A	GRCh37
NC_000017.9:g.19753167T>A	NCBI36
NG_011493.1:g.73555A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225737.11:c.1902A>T MANE Select	ENSP00000225737.6:p.Leu634=
ENST00000225737.10:c.1902A>T	ENSP00000225737.6:p.Leu634=
ENST00000395536.7:c.1728A>T	ENSP00000378907.3:p.Leu576=
ENST00000578898.1:c.329A>T
ENST00000583951.1:c.213A>T	ENSP00000463398.1:p.Leu71=
NM_007202.3:c.1902A>T	NP_009133.2:p.Leu634=
XM_006721431.2:c.1835-3030A>T	XP_006721494.1:n.1835-3030A>T
XM_006721432.2:c.1728A>T	XP_006721495.1:p.Leu576=
XR_933969.1:n.1950A>T
XR_933970.1:n.1883-3030A>T
NM_001330152.1:c.1728A>T	NP_001317081.1:p.Leu576=
XR_001752418.2:n.2014A>T
XR_933969.3:n.1933A>T
NM_007202.4:c.1902A>T MANE Select	NP_009133.2:p.Leu634=
NM_001330152.2:c.1728A>T	NP_001317081.1:p.Leu576=