Canonical Allele Identifier: CA44486284

Gene: ATRAID

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27217151del , CM000664.2:g.27217151del	GRCh38
NC_000002.11:g.27440019del , CM000664.1:g.27440019del	GRCh37
NC_000002.10:g.27293523del	NCBI36
NG_046394.1:g.4762del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380171.9:c.*203del MANE Select	ENSP00000369518.4:n.*203del
ENST00000380171.8:c.*203del	ENSP00000369518.4:n.*203del
ENST00000380171.7:c.*203del	ENSP00000369518.3:n.*203del
ENST00000405489.7:c.*203del	ENSP00000384033.3:n.*203del
ENST00000472515.1:n.555del
ENST00000606999.5:c.*203del	ENSP00000476080.1:n.*203del
ENST00000611786.4:c.*203del	ENSP00000484228.1:n.*203del
NM_001170795.1:c.*203del	NP_001164266.1:n.*203del
NM_016085.4:c.*203del	NP_057169.2:n.*203del
NM_080592.3:c.*203del	NP_542159.3:n.*203del
NM_001170795.3:c.*203del	NP_001164266.1:n.*203del
NM_016085.5:c.*203del	NP_057169.2:n.*203del
NM_001170795.4:c.*203del MANE Select	NP_001164266.1:n.*203del