Canonical Allele Identifier: CA490434387

Gene: DNAAF4 DNAAF4-CCPG1

Linked Data

• MyVariant Identifiers: chr15:g.55783393T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.55491195T>G , CM000677.2:g.55491195T>G	GRCh38
NC_000015.9:g.55783393T>G , CM000677.1:g.55783393T>G	GRCh37
NC_000015.8:g.53570685T>G	NCBI36
NG_021213.1:g.22040A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321149.7:c.333A>C (DNAAF4) MANE Select	ENSP00000323275.3:p.Ala111=
ENST00000348518.4:c.333A>C (DNAAF4)	ENSP00000299561.5:p.Ala111=
ENST00000448430.6:c.333A>C (DNAAF4)	ENSP00000403412.2:p.Ala111=
ENST00000457155.6:c.333A>C (DNAAF4)	ENSP00000402640.2:p.Ala111=
ENST00000519017.1:n.348A>C (DNAAF4)
ENST00000522437.1:c.*143A>C (DNAAF4)	ENSP00000429219.1:n.*143A>C
ENST00000524160.5:c.333A>C (DNAAF4)	ENSP00000428097.1:p.Ala111=
NM_001033559.2:c.333A>C (DNAAF4)	NP_001028731.1:p.Ala111=
NM_001033560.1:c.333A>C (DNAAF4)	NP_001028732.1:p.Ala111=
NM_130810.3:c.333A>C (DNAAF4)	NP_570722.2:p.Ala111=
NR_037923.1:n.588A>C (DNAAF4-CCPG1)
NM_130810.4:c.333A>C (DNAAF4) MANE Select	NP_570722.2:p.Ala111=
NM_001033559.3:c.333A>C (DNAAF4)	NP_001028731.1:p.Ala111=
NM_001033560.2:c.333A>C (DNAAF4)	NP_001028732.1:p.Ala111=