Canonical Allele Identifier: CA413189050
Gene: AKAP4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50192792T>C , CM000685.2:g.50192792T>C GRCh38
NC_000023.10:g.49957443T>C , CM000685.1:g.49957443T>C GRCh37
NC_000023.9:g.49844183T>C NCBI36
NG_012552.1:g.13222A>G
NG_012552.2:g.13222A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000358526.7:c.1921A>G MANE Select ENSP00000351327.2:p.Asn641Asp
ENST00000358526.6:c.1921A>G ENSP00000351327.2:p.Asn641Asp
ENST00000376064.7:c.1894A>G ENSP00000365232.3:p.Asn632Asp
ENST00000481402.5:n.2033A>G
NM_003886.2:c.1921A>G NP_003877.2:p.Asn641Asp
NM_139289.1:c.1894A>G NP_647450.1:p.Asn632Asp
NM_003886.3:c.1921A>G MANE Select NP_003877.2:p.Asn641Asp
NM_139289.2:c.1894A>G NP_647450.1:p.Asn632Asp