Canonical Allele Identifier: CA516680044
Gene: AKAP4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.49957240G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50192589G>A , CM000685.2:g.50192589G>A GRCh38
NC_000023.10:g.49957240G>A , CM000685.1:g.49957240G>A GRCh37
NC_000023.9:g.49843980G>A NCBI36
NG_012552.1:g.13425C>T
NG_012552.2:g.13425C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000358526.7:c.2124C>T MANE Select ENSP00000351327.2:p.Cys708=
ENST00000358526.6:c.2124C>T ENSP00000351327.2:p.Cys708=
ENST00000376064.7:c.2097C>T ENSP00000365232.3:p.Cys699=
ENST00000481402.5:n.2236C>T
NM_003886.2:c.2124C>T NP_003877.2:p.Cys708=
NM_139289.1:c.2097C>T NP_647450.1:p.Cys699=
NM_003886.3:c.2124C>T MANE Select NP_003877.2:p.Cys708=
NM_139289.2:c.2097C>T NP_647450.1:p.Cys699=