Canonical Allele Identifier: CA10414181
Gene: AKAP4 HGNC NCBI

Linked Data

dbSNP Id: rs782186826
gnomAD v2: X-49957679-C-A
gnomAD v3: X-50193028-C-A
gnomAD v4: X-50193028-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50193028C>A , CM000685.2:g.50193028C>A GRCh38
NC_000023.10:g.49957679C>A , CM000685.1:g.49957679C>A GRCh37
NC_000023.9:g.49844419C>A NCBI36
NG_012552.1:g.12986G>T
NG_012552.2:g.12986G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000358526.7:c.1685G>T MANE Select ENSP00000351327.2:p.Gly562Val
ENST00000358526.6:c.1685G>T ENSP00000351327.2:p.Gly562Val
ENST00000376064.7:c.1658G>T ENSP00000365232.3:p.Gly553Val
ENST00000448865.5:c.542-6G>T ENSP00000402403.1:n.542-6G>T
ENST00000481402.5:n.1797G>T
NM_003886.2:c.1685G>T NP_003877.2:p.Gly562Val
NM_139289.1:c.1658G>T NP_647450.1:p.Gly553Val
NM_003886.3:c.1685G>T MANE Select NP_003877.2:p.Gly562Val
NM_139289.2:c.1658G>T NP_647450.1:p.Gly553Val