Canonical Allele Identifier: CA398726171
Gene: AKAP10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19909245T>G , CM000679.2:g.19909245T>G GRCh38
NC_000017.10:g.19812558T>G , CM000679.1:g.19812558T>G GRCh37
NC_000017.9:g.19753150T>G NCBI36
NG_011493.1:g.73572A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000225737.11:c.1919A>C MANE Select ENSP00000225737.6:p.Lys640Thr
ENST00000225737.10:c.1919A>C ENSP00000225737.6:p.Lys640Thr
ENST00000395536.7:c.1745A>C ENSP00000378907.3:p.Lys582Thr
ENST00000578898.1:c.346A>C
ENST00000583951.1:c.230A>C ENSP00000463398.1:p.Lys77Thr
NM_007202.3:c.1919A>C NP_009133.2:p.Lys640Thr
XM_006721431.2:c.1835-3013A>C XP_006721494.1:n.1835-3013A>C
XM_006721432.2:c.1745A>C XP_006721495.1:p.Lys582Thr
XR_933969.1:n.1967A>C
XR_933970.1:n.1883-3013A>C
NM_001330152.1:c.1745A>C NP_001317081.1:p.Lys582Thr
XR_001752418.2:n.2031A>C
XR_933969.3:n.1950A>C
NM_007202.4:c.1919A>C MANE Select NP_009133.2:p.Lys640Thr
NM_001330152.2:c.1745A>C NP_001317081.1:p.Lys582Thr