Canonical Allele Identifier: CA413187425
Gene: AKAP4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.49957022A>G (hg19) chrX:g.50192371A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50192371A>G , CM000685.2:g.50192371A>G GRCh38
NC_000023.10:g.49957022A>G , CM000685.1:g.49957022A>G GRCh37
NC_000023.9:g.49843762A>G NCBI36
NG_012552.1:g.13643T>C
NG_012552.2:g.13643T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000358526.7:c.2342T>C MANE Select ENSP00000351327.2:p.Ile781Thr
ENST00000358526.6:c.2342T>C ENSP00000351327.2:p.Ile781Thr
ENST00000376064.7:c.2315T>C ENSP00000365232.3:p.Ile772Thr
ENST00000481402.5:n.2454T>C
NM_003886.2:c.2342T>C NP_003877.2:p.Ile781Thr
NM_139289.1:c.2315T>C NP_647450.1:p.Ile772Thr
NM_003886.3:c.2342T>C MANE Select NP_003877.2:p.Ile781Thr
NM_139289.2:c.2315T>C NP_647450.1:p.Ile772Thr
Search 100 bp 5'
Search 100 bp 3'