Canonical Allele Identifier: CA2178869301

Gene: DNAAF4 DNAAF4-CCPG1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.55491143C= , CM000677.2:g.55491143C=	GRCh38
NC_000015.9:g.55783341C= , CM000677.1:g.55783341C=	GRCh37
NC_000015.8:g.53570633C=	NCBI36
NG_021213.1:g.22092G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321149.7:c.385G= (DNAAF4) MANE Select	ENSP00000323275.3:p.Ala129=
ENST00000348518.4:c.385G= (DNAAF4)	ENSP00000299561.5:p.Ala129=
ENST00000448430.6:c.385G= (DNAAF4)	ENSP00000403412.2:p.Ala129=
ENST00000457155.6:c.385G= (DNAAF4)	ENSP00000402640.2:p.Ala129=
ENST00000519017.1:n.400G= (DNAAF4)
ENST00000522437.1:c.*195G= (DNAAF4)	ENSP00000429219.1:n.*195G=
ENST00000524160.5:c.385G= (DNAAF4)	ENSP00000428097.1:p.Ala129=
NM_001033559.2:c.385G= (DNAAF4)	NP_001028731.1:p.Ala129=
NM_001033560.1:c.385G= (DNAAF4)	NP_001028732.1:p.Ala129=
NM_130810.3:c.385G= (DNAAF4)	NP_570722.2:p.Ala129=
NR_037923.1:n.640G= (DNAAF4-CCPG1)
NM_130810.4:c.385G= (DNAAF4) MANE Select	NP_570722.2:p.Ala129=
NM_001033559.3:c.385G= (DNAAF4)	NP_001028731.1:p.Ala129=
NM_001033560.2:c.385G= (DNAAF4)	NP_001028732.1:p.Ala129=