Canonical Allele Identifier: CA407447055

Gene: DNAAF3 DNAAF3-AS1

Linked Data

• MyVariant Identifiers: chr19:g.55670717G>A (hg19) ; chr19:g.55159349G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55159349G>A , CM000681.2:g.55159349G>A	GRCh38
NC_000019.9:g.55670717G>A , CM000681.1:g.55670717G>A	GRCh37
NC_000019.8:g.60362529G>A	NCBI36
NG_007866.2:g.3384C>T , LRG_432:g.3384C>T
NG_032759.1:g.12374C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000524407.7:c.1339C>T (DNAAF3) MANE Select	ENSP00000432046.3:p.Pro447Ser
ENST00000391720.8:c.1480C>T (DNAAF3)	ENSP00000375600.5:p.Pro494Ser
ENST00000455045.5:c.1177C>T (DNAAF3)	ENSP00000394343.1:p.Pro393Ser
ENST00000524407.6:c.1339C>T (DNAAF3)	ENSP00000432046.2:p.Pro447Ser
ENST00000527223.6:c.1540C>T (DNAAF3)	ENSP00000436975.2:p.Pro514Ser
ENST00000528412.5:c.*1127C>T (DNAAF3)	ENSP00000433826.2:n.*1127C>T
ENST00000533527.6:n.1101C>T (DNAAF3)
ENST00000587789.2:n.424C>T (DNAAF3)
ENST00000587871.1:c.323C>T
ENST00000588076.1:c.338C>T (DNAAF3)
NM_001256714.1:c.1540C>T (DNAAF3)	NP_001243643.1:p.Pro514Ser
NM_001256715.1:c.1339C>T (DNAAF3)	NP_001243644.1:p.Pro447Ser
NM_001256716.1:c.1177C>T (DNAAF3)	NP_001243645.1:p.Pro393Ser
NM_178837.4:c.1480C>T (DNAAF3)	NP_849159.2:p.Pro494Ser
XR_001754015.1:n.11G>A (DNAAF3-AS1)
NM_001256715.2:c.1339C>T (DNAAF3) MANE Select	NP_001243644.1:p.Pro447Ser
NM_001256716.2:c.1177C>T (DNAAF3)	NP_001243645.1:p.Pro393Ser