Canonical Allele Identifier: CA7575069
Gene: DNAAF4 HGNC NCBI
DNAAF4-CCPG1 HGNC NCBI

Linked Data

dbSNP Id: rs770568793

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.55491173C>T , CM000677.2:g.55491173C>T GRCh38
NC_000015.9:g.55783371C>T , CM000677.1:g.55783371C>T GRCh37
NC_000015.8:g.53570663C>T NCBI36
NG_021213.1:g.22062G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000321149.7:c.355G>A (DNAAF4) MANE Select ENSP00000323275.3:p.Ala119Thr
ENST00000348518.4:c.355G>A (DNAAF4) ENSP00000299561.5:p.Ala119Thr
ENST00000448430.6:c.355G>A (DNAAF4) ENSP00000403412.2:p.Ala119Thr
ENST00000457155.6:c.355G>A (DNAAF4) ENSP00000402640.2:p.Ala119Thr
ENST00000519017.1:n.370G>A (DNAAF4)
ENST00000522437.1:c.*165G>A (DNAAF4) ENSP00000429219.1:n.*165G>A
ENST00000524160.5:c.355G>A (DNAAF4) ENSP00000428097.1:p.Ala119Thr
NM_001033559.2:c.355G>A (DNAAF4) NP_001028731.1:p.Ala119Thr
NM_001033560.1:c.355G>A (DNAAF4) NP_001028732.1:p.Ala119Thr
NM_130810.3:c.355G>A (DNAAF4) NP_570722.2:p.Ala119Thr
NR_037923.1:n.610G>A (DNAAF4-CCPG1)
NM_130810.4:c.355G>A (DNAAF4) MANE Select NP_570722.2:p.Ala119Thr
NM_001033559.3:c.355G>A (DNAAF4) NP_001028731.1:p.Ala119Thr
NM_001033560.2:c.355G>A (DNAAF4) NP_001028732.1:p.Ala119Thr