Canonical Allele Identifier: CA413188169
Gene: AKAP4 HGNC NCBI

Linked Data

dbSNP Id: rs2146961450

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50192595C>A , CM000685.2:g.50192595C>A GRCh38
NC_000023.10:g.49957246C>A , CM000685.1:g.49957246C>A GRCh37
NC_000023.9:g.49843986C>A NCBI36
NG_012552.1:g.13419G>T
NG_012552.2:g.13419G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000358526.7:c.2118G>T MANE Select ENSP00000351327.2:p.Lys706Asn
ENST00000358526.6:c.2118G>T ENSP00000351327.2:p.Lys706Asn
ENST00000376064.7:c.2091G>T ENSP00000365232.3:p.Lys697Asn
ENST00000481402.5:n.2230G>T
NM_003886.2:c.2118G>T NP_003877.2:p.Lys706Asn
NM_139289.1:c.2091G>T NP_647450.1:p.Lys697Asn
NM_003886.3:c.2118G>T MANE Select NP_003877.2:p.Lys706Asn
NM_139289.2:c.2091G>T NP_647450.1:p.Lys697Asn