Canonical Allele Identifier: CA516679223
Gene: AKAP4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.49957354A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50192703A>T , CM000685.2:g.50192703A>T GRCh38
NC_000023.10:g.49957354A>T , CM000685.1:g.49957354A>T GRCh37
NC_000023.9:g.49844094A>T NCBI36
NG_012552.1:g.13311T>A
NG_012552.2:g.13311T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000358526.7:c.2010T>A MANE Select ENSP00000351327.2:p.Ser670=
ENST00000358526.6:c.2010T>A ENSP00000351327.2:p.Ser670=
ENST00000376064.7:c.1983T>A ENSP00000365232.3:p.Ser661=
ENST00000481402.5:n.2122T>A
NM_003886.2:c.2010T>A NP_003877.2:p.Ser670=
NM_139289.1:c.1983T>A NP_647450.1:p.Ser661=
NM_003886.3:c.2010T>A MANE Select NP_003877.2:p.Ser670=
NM_139289.2:c.1983T>A NP_647450.1:p.Ser661=