Canonical Allele Identifier: CA413188062
Gene: AKAP4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50192571A>C , CM000685.2:g.50192571A>C GRCh38
NC_000023.10:g.49957222A>C , CM000685.1:g.49957222A>C GRCh37
NC_000023.9:g.49843962A>C NCBI36
NG_012552.1:g.13443T>G
NG_012552.2:g.13443T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000358526.7:c.2142T>G MANE Select ENSP00000351327.2:p.Tyr714Ter
ENST00000358526.6:c.2142T>G ENSP00000351327.2:p.Tyr714Ter
ENST00000376064.7:c.2115T>G ENSP00000365232.3:p.Tyr705Ter
ENST00000481402.5:n.2254T>G
NM_003886.2:c.2142T>G NP_003877.2:p.Tyr714Ter
NM_139289.1:c.2115T>G NP_647450.1:p.Tyr705Ter
NM_003886.3:c.2142T>G MANE Select NP_003877.2:p.Tyr714Ter
NM_139289.2:c.2115T>G NP_647450.1:p.Tyr705Ter