Canonical Allele Identifier: CA413189585
Gene: AKAP4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50192911A>C , CM000685.2:g.50192911A>C GRCh38
NC_000023.10:g.49957562A>C , CM000685.1:g.49957562A>C GRCh37
NC_000023.9:g.49844302A>C NCBI36
NG_012552.1:g.13103T>G
NG_012552.2:g.13103T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000358526.7:c.1802T>G MANE Select ENSP00000351327.2:p.Leu601Arg
ENST00000358526.6:c.1802T>G ENSP00000351327.2:p.Leu601Arg
ENST00000376064.7:c.1775T>G ENSP00000365232.3:p.Leu592Arg
ENST00000481402.5:n.1914T>G
NM_003886.2:c.1802T>G NP_003877.2:p.Leu601Arg
NM_139289.1:c.1775T>G NP_647450.1:p.Leu592Arg
NM_003886.3:c.1802T>G MANE Select NP_003877.2:p.Leu601Arg
NM_139289.2:c.1775T>G NP_647450.1:p.Leu592Arg