Canonical Allele Identifier: CA200549

Gene: DNAAF2

Linked Data

• ClinVar Variation Id: 193393
• ClinVar RCV Id: RCV000173463 ; RCV000196382 ; RCV001111756 ; RCV003389758
• dbSNP Id: rs144077436
• ExAC: 14:50100284 A / T
• gnomAD v2: 14-50100284-A-T
• gnomAD v3: 14-49633566-A-T
• gnomAD v4: 14-49633566-A-T
• MyVariant Identifiers: chr14:g.50100284A>T (hg19) ; chr14:g.49633566A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.49633566A>T , CM000676.2:g.49633566A>T	GRCh38
NC_000014.8:g.50100284A>T , CM000676.1:g.50100284A>T	GRCh37
NC_000014.7:g.49170034A>T	NCBI36
NG_013070.1:g.6665T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298292.13:c.1584T>A MANE Select	ENSP00000298292.8:p.Asn528Lys
ENST00000298292.12:c.1584T>A	ENSP00000298292.8:p.Asn528Lys
ENST00000406043.3:c.1584T>A	ENSP00000384862.3:p.Asn528Lys
NM_001083908.1:c.1584T>A	NP_001077377.1:p.Asn528Lys
NM_018139.2:c.1584T>A	NP_060609.2:p.Asn528Lys
NM_001083908.2:c.1584T>A	NP_001077377.1:p.Asn528Lys
NM_001378453.1:c.-288T>A	NP_001365382.1:n.-288T>A
NM_018139.3:c.1584T>A MANE Select	NP_060609.2:p.Asn528Lys