Canonical Allele Identifier: CA413189229
Gene: AKAP4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50192834A>C , CM000685.2:g.50192834A>C GRCh38
NC_000023.10:g.49957485A>C , CM000685.1:g.49957485A>C GRCh37
NC_000023.9:g.49844225A>C NCBI36
NG_012552.1:g.13180T>G
NG_012552.2:g.13180T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000358526.7:c.1879T>G MANE Select ENSP00000351327.2:p.Ser627Ala
ENST00000358526.6:c.1879T>G ENSP00000351327.2:p.Ser627Ala
ENST00000376064.7:c.1852T>G ENSP00000365232.3:p.Ser618Ala
ENST00000481402.5:n.1991T>G
NM_003886.2:c.1879T>G NP_003877.2:p.Ser627Ala
NM_139289.1:c.1852T>G NP_647450.1:p.Ser618Ala
NM_003886.3:c.1879T>G MANE Select NP_003877.2:p.Ser627Ala
NM_139289.2:c.1852T>G NP_647450.1:p.Ser618Ala