Canonical Allele Identifier: CA509195937
Gene: DNAAF3 HGNC NCBI
DNAAF3-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.55670821C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55159453C>A , CM000681.2:g.55159453C>A GRCh38
NC_000019.9:g.55670821C>A , CM000681.1:g.55670821C>A GRCh37
NC_000019.8:g.60362633C>A NCBI36
NG_007866.2:g.3280G>T , LRG_432:g.3280G>T
NG_032759.1:g.12270G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000524407.7:c.1239-4G>T (DNAAF3) MANE Select ENSP00000432046.3:n.1239-4G>T
ENST00000391720.8:c.1380-4G>T (DNAAF3) ENSP00000375600.5:n.1380-4G>T
ENST00000455045.5:c.1077-4G>T (DNAAF3) ENSP00000394343.1:n.1077-4G>T
ENST00000524407.6:c.1239-4G>T (DNAAF3) ENSP00000432046.2:n.1239-4G>T
ENST00000527223.6:c.1440-4G>T (DNAAF3) ENSP00000436975.2:n.1440-4G>T
ENST00000528412.5:c.*1027-4G>T (DNAAF3) ENSP00000433826.2:n.*1027-4G>T
ENST00000533527.6:n.1001-4G>T (DNAAF3)
ENST00000587789.2:n.324-4G>T (DNAAF3)
ENST00000587871.1:c.223-4G>T
ENST00000588076.1:c.238-4G>T (DNAAF3)
NM_001256714.1:c.1440-4G>T (DNAAF3) NP_001243643.1:n.1440-4G>T
NM_001256715.1:c.1239-4G>T (DNAAF3) NP_001243644.1:n.1239-4G>T
NM_001256716.1:c.1077-4G>T (DNAAF3) NP_001243645.1:n.1077-4G>T
NM_178837.4:c.1380-4G>T (DNAAF3) NP_849159.2:n.1380-4G>T
XR_001754014.1:n.87+8C>A (DNAAF3-AS1)
XR_001754015.1:n.107+8C>A (DNAAF3-AS1)
NM_001256715.2:c.1239-4G>T (DNAAF3) MANE Select NP_001243644.1:n.1239-4G>T
NM_001256716.2:c.1077-4G>T (DNAAF3) NP_001243645.1:n.1077-4G>T