Canonical Allele Identifier: CA392553131
Gene: DNAAF4 HGNC NCBI
DNAAF4-CCPG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.55497828A>C , CM000677.2:g.55497828A>C GRCh38
NC_000015.9:g.55790026A>C , CM000677.1:g.55790026A>C GRCh37
NC_000015.8:g.53577318A>C NCBI36
NG_021213.1:g.15407T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000321149.7:c.155T>G (DNAAF4) MANE Select ENSP00000323275.3:p.Phe52Cys
ENST00000348518.4:c.155T>G (DNAAF4) ENSP00000299561.5:p.Phe52Cys
ENST00000448430.6:c.155T>G (DNAAF4) ENSP00000403412.2:p.Phe52Cys
ENST00000457155.6:c.155T>G (DNAAF4) ENSP00000402640.2:p.Phe52Cys
ENST00000519017.1:n.170T>G (DNAAF4)
ENST00000522437.1:c.124-18T>G (DNAAF4) ENSP00000429219.1:n.124-18T>G
ENST00000524160.5:c.155T>G (DNAAF4) ENSP00000428097.1:p.Phe52Cys
NM_001033559.2:c.155T>G (DNAAF4) NP_001028731.1:p.Phe52Cys
NM_001033560.1:c.155T>G (DNAAF4) NP_001028732.1:p.Phe52Cys
NM_130810.3:c.155T>G (DNAAF4) NP_570722.2:p.Phe52Cys
NR_037923.1:n.410T>G (DNAAF4-CCPG1)
NM_130810.4:c.155T>G (DNAAF4) MANE Select NP_570722.2:p.Phe52Cys
NM_001033559.3:c.155T>G (DNAAF4) NP_001028731.1:p.Phe52Cys
NM_001033560.2:c.155T>G (DNAAF4) NP_001028732.1:p.Phe52Cys