Canonical Allele Identifier: CA413189079
Gene: AKAP4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50192798T>A , CM000685.2:g.50192798T>A GRCh38
NC_000023.10:g.49957449T>A , CM000685.1:g.49957449T>A GRCh37
NC_000023.9:g.49844189T>A NCBI36
NG_012552.1:g.13216A>T
NG_012552.2:g.13216A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000358526.7:c.1915A>T MANE Select ENSP00000351327.2:p.Asn639Tyr
ENST00000358526.6:c.1915A>T ENSP00000351327.2:p.Asn639Tyr
ENST00000376064.7:c.1888A>T ENSP00000365232.3:p.Asn630Tyr
ENST00000481402.5:n.2027A>T
NM_003886.2:c.1915A>T NP_003877.2:p.Asn639Tyr
NM_139289.1:c.1888A>T NP_647450.1:p.Asn630Tyr
NM_003886.3:c.1915A>T MANE Select NP_003877.2:p.Asn639Tyr
NM_139289.2:c.1888A>T NP_647450.1:p.Asn630Tyr