Canonical Allele Identifier: CA407447111

Gene: DNAAF3 DNAAF3-AS1

Linked Data

• dbSNP Id: rs768592462
• COSMIC: COSM6086037 ; COSM6086038 ; COSM6086039
• MyVariant Identifiers: chr19:g.55670723C>A (hg19) ; chr19:g.55159355C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55159355C>A , CM000681.2:g.55159355C>A	GRCh38
NC_000019.9:g.55670723C>A , CM000681.1:g.55670723C>A	GRCh37
NC_000019.8:g.60362535C>A	NCBI36
NG_007866.2:g.3378G>T , LRG_432:g.3378G>T
NG_032759.1:g.12368G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000524407.7:c.1333G>T (DNAAF3) MANE Select	ENSP00000432046.3:p.Ala445Ser
ENST00000391720.8:c.1474G>T (DNAAF3)	ENSP00000375600.5:p.Ala492Ser
ENST00000455045.5:c.1171G>T (DNAAF3)	ENSP00000394343.1:p.Ala391Ser
ENST00000524407.6:c.1333G>T (DNAAF3)	ENSP00000432046.2:p.Ala445Ser
ENST00000527223.6:c.1534G>T (DNAAF3)	ENSP00000436975.2:p.Ala512Ser
ENST00000528412.5:c.*1121G>T (DNAAF3)	ENSP00000433826.2:n.*1121G>T
ENST00000533527.6:n.1095G>T (DNAAF3)
ENST00000587789.2:n.418G>T (DNAAF3)
ENST00000587871.1:c.317G>T
ENST00000588076.1:c.332G>T (DNAAF3)
NM_001256714.1:c.1534G>T (DNAAF3)	NP_001243643.1:p.Ala512Ser
NM_001256715.1:c.1333G>T (DNAAF3)	NP_001243644.1:p.Ala445Ser
NM_001256716.1:c.1171G>T (DNAAF3)	NP_001243645.1:p.Ala391Ser
NM_178837.4:c.1474G>T (DNAAF3)	NP_849159.2:p.Ala492Ser
XR_001754015.1:n.17C>A (DNAAF3-AS1)
NM_001256715.2:c.1333G>T (DNAAF3) MANE Select	NP_001243644.1:p.Ala445Ser
NM_001256716.2:c.1171G>T (DNAAF3)	NP_001243645.1:p.Ala391Ser