Canonical Allele Identifier: CA413188421
Gene: AKAP4 HGNC NCBI

Linked Data

COSMIC: COSM457666

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50192647A>T , CM000685.2:g.50192647A>T GRCh38
NC_000023.10:g.49957298A>T , CM000685.1:g.49957298A>T GRCh37
NC_000023.9:g.49844038A>T NCBI36
NG_012552.1:g.13367T>A
NG_012552.2:g.13367T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000358526.7:c.2066T>A MANE Select ENSP00000351327.2:p.Met689Lys
ENST00000358526.6:c.2066T>A ENSP00000351327.2:p.Met689Lys
ENST00000376064.7:c.2039T>A ENSP00000365232.3:p.Met680Lys
ENST00000481402.5:n.2178T>A
NM_003886.2:c.2066T>A NP_003877.2:p.Met689Lys
NM_139289.1:c.2039T>A NP_647450.1:p.Met680Lys
NM_003886.3:c.2066T>A MANE Select NP_003877.2:p.Met689Lys
NM_139289.2:c.2039T>A NP_647450.1:p.Met680Lys