Canonical Allele Identifier: CA413187501
Gene: AKAP4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.49957049T>C (hg19) chrX:g.50192398T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50192398T>C , CM000685.2:g.50192398T>C GRCh38
NC_000023.10:g.49957049T>C , CM000685.1:g.49957049T>C GRCh37
NC_000023.9:g.49843789T>C NCBI36
NG_012552.1:g.13616A>G
NG_012552.2:g.13616A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000358526.7:c.2315A>G MANE Select ENSP00000351327.2:p.Lys772Arg
ENST00000358526.6:c.2315A>G ENSP00000351327.2:p.Lys772Arg
ENST00000376064.7:c.2288A>G ENSP00000365232.3:p.Lys763Arg
ENST00000481402.5:n.2427A>G
NM_003886.2:c.2315A>G NP_003877.2:p.Lys772Arg
NM_139289.1:c.2288A>G NP_647450.1:p.Lys763Arg
NM_003886.3:c.2315A>G MANE Select NP_003877.2:p.Lys772Arg
NM_139289.2:c.2288A>G NP_647450.1:p.Lys763Arg
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Search 100 bp 3'