Canonical Allele Identifier: CA9668269

Gene: DNAAF3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55166363C>T , CM000681.2:g.55166363C>T	GRCh38
NC_000019.9:g.55677731C>T , CM000681.1:g.55677731C>T	GRCh37
NC_000019.8:g.60369543C>T	NCBI36
NG_032759.1:g.5360G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001256715.2:c.51G>A MANE Select	NP_001243644.1:p.Trp17Ter
ENST00000524407.7:c.51G>A MANE Select	ENSP00000432046.3:p.Trp17Ter
NM_001256714.1:c.192G>A	NP_001243643.1:p.Trp64Ter
NM_001256715.1:c.51G>A	NP_001243644.1:p.Trp17Ter
NM_001256716.1:c.-188G>A	NP_001243645.1:n.-188G>A
NM_001256716.2:c.-188G>A	NP_001243645.1:n.-188G>A
NM_178837.4:c.192G>A	NP_849159.2:p.Trp64Ter
ENST00000391720.8:c.192G>A	ENSP00000375600.5:p.Trp64Ter
ENST00000455045.5:c.-188G>A	ENSP00000394343.1:n.-188G>A
ENST00000524407.6:c.51G>A	ENSP00000432046.2:p.Trp17Ter
ENST00000526003.5:c.51G>A	ENSP00000473009.1:p.Trp17Ter
ENST00000527223.6:c.192G>A	ENSP00000436975.2:p.Trp64Ter
ENST00000528412.5:c.51G>A	ENSP00000433826.2:p.Trp17Ter
ENST00000528476.1:n.266G>A
ENST00000532817.5:c.-81G>A	ENSP00000432838.2:n.-81G>A
ENST00000534170.5:c.-81G>A	ENSP00000432360.2:n.-81G>A
ENST00000534214.1:c.51G>A	ENSP00000433247.2:p.Trp17Ter
ENST00000586877.1:n.173G>A