Canonical Allele Identifier: CA498642264
Gene: AKAP10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.19812577G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19909264G>A , CM000679.2:g.19909264G>A GRCh38
NC_000017.10:g.19812577G>A , CM000679.1:g.19812577G>A GRCh37
NC_000017.9:g.19753169G>A NCBI36
NG_011493.1:g.73553C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000225737.11:c.1900C>T MANE Select ENSP00000225737.6:p.Leu634=
ENST00000225737.10:c.1900C>T ENSP00000225737.6:p.Leu634=
ENST00000395536.7:c.1726C>T ENSP00000378907.3:p.Leu576=
ENST00000578898.1:c.327C>T
ENST00000583951.1:c.211C>T ENSP00000463398.1:p.Leu71=
NM_007202.3:c.1900C>T NP_009133.2:p.Leu634=
XM_006721431.2:c.1835-3032C>T XP_006721494.1:n.1835-3032C>T
XM_006721432.2:c.1726C>T XP_006721495.1:p.Leu576=
XR_933969.1:n.1948C>T
XR_933970.1:n.1883-3032C>T
NM_001330152.1:c.1726C>T NP_001317081.1:p.Leu576=
XR_001752418.2:n.2012C>T
XR_933969.3:n.1931C>T
NM_007202.4:c.1900C>T MANE Select NP_009133.2:p.Leu634=
NM_001330152.2:c.1726C>T NP_001317081.1:p.Leu576=