Canonical Allele Identifier: CA413187591
Gene: AKAP4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.49957086T>G (hg19) chrX:g.50192435T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50192435T>G , CM000685.2:g.50192435T>G GRCh38
NC_000023.10:g.49957086T>G , CM000685.1:g.49957086T>G GRCh37
NC_000023.9:g.49843826T>G NCBI36
NG_012552.1:g.13579A>C
NG_012552.2:g.13579A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000358526.7:c.2278A>C MANE Select ENSP00000351327.2:p.Ile760Leu
ENST00000358526.6:c.2278A>C ENSP00000351327.2:p.Ile760Leu
ENST00000376064.7:c.2251A>C ENSP00000365232.3:p.Ile751Leu
ENST00000481402.5:n.2390A>C
NM_003886.2:c.2278A>C NP_003877.2:p.Ile760Leu
NM_139289.1:c.2251A>C NP_647450.1:p.Ile751Leu
NM_003886.3:c.2278A>C MANE Select NP_003877.2:p.Ile760Leu
NM_139289.2:c.2251A>C NP_647450.1:p.Ile751Leu
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