Canonical Allele Identifier: CA509195714
Gene: DNAAF3 HGNC NCBI
DNAAF3-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.55670721G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55159353G>T , CM000681.2:g.55159353G>T GRCh38
NC_000019.9:g.55670721G>T , CM000681.1:g.55670721G>T GRCh37
NC_000019.8:g.60362533G>T NCBI36
NG_007866.2:g.3380C>A , LRG_432:g.3380C>A
NG_032759.1:g.12370C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000524407.7:c.1335C>A (DNAAF3) MANE Select ENSP00000432046.3:p.Ala445=
ENST00000391720.8:c.1476C>A (DNAAF3) ENSP00000375600.5:p.Ala492=
ENST00000455045.5:c.1173C>A (DNAAF3) ENSP00000394343.1:p.Ala391=
ENST00000524407.6:c.1335C>A (DNAAF3) ENSP00000432046.2:p.Ala445=
ENST00000527223.6:c.1536C>A (DNAAF3) ENSP00000436975.2:p.Ala512=
ENST00000528412.5:c.*1123C>A (DNAAF3) ENSP00000433826.2:n.*1123C>A
ENST00000533527.6:n.1097C>A (DNAAF3)
ENST00000587789.2:n.420C>A (DNAAF3)
ENST00000587871.1:c.319C>A
ENST00000588076.1:c.334C>A (DNAAF3)
NM_001256714.1:c.1536C>A (DNAAF3) NP_001243643.1:p.Ala512=
NM_001256715.1:c.1335C>A (DNAAF3) NP_001243644.1:p.Ala445=
NM_001256716.1:c.1173C>A (DNAAF3) NP_001243645.1:p.Ala391=
NM_178837.4:c.1476C>A (DNAAF3) NP_849159.2:p.Ala492=
XR_001754015.1:n.15G>T (DNAAF3-AS1)
NM_001256715.2:c.1335C>A (DNAAF3) MANE Select NP_001243644.1:p.Ala445=
NM_001256716.2:c.1173C>A (DNAAF3) NP_001243645.1:p.Ala391=