Canonical Allele Identifier: CA413188667
Gene: AKAP4 HGNC NCBI

Linked Data

gnomAD v4: X-50192709-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50192709G>T , CM000685.2:g.50192709G>T GRCh38
NC_000023.10:g.49957360G>T , CM000685.1:g.49957360G>T GRCh37
NC_000023.9:g.49844100G>T NCBI36
NG_012552.1:g.13305C>A
NG_012552.2:g.13305C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000358526.7:c.2004C>A MANE Select ENSP00000351327.2:p.Asn668Lys
ENST00000358526.6:c.2004C>A ENSP00000351327.2:p.Asn668Lys
ENST00000376064.7:c.1977C>A ENSP00000365232.3:p.Asn659Lys
ENST00000481402.5:n.2116C>A
NM_003886.2:c.2004C>A NP_003877.2:p.Asn668Lys
NM_139289.1:c.1977C>A NP_647450.1:p.Asn659Lys
NM_003886.3:c.2004C>A MANE Select NP_003877.2:p.Asn668Lys
NM_139289.2:c.1977C>A NP_647450.1:p.Asn659Lys