Canonical Allele Identifier: CA2841294349

Gene: CYBA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88643343_88643344insA , CM000678.2:g.88643343_88643344insA	GRCh38
NC_000016.9:g.88709751_88709752insA , CM000678.1:g.88709751_88709752insA	GRCh37
NC_000016.8:g.87237252_87237253insA	NCBI36
NG_007291.1:g.12706_12707insT , LRG_52:g.12706_12707insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696156.1:c.*9_*10insT	ENSP00000512446.1:n.*9_*10insT
ENST00000696157.1:c.*814_*815insT	ENSP00000512447.1:n.*814_*815insT
ENST00000696158.1:c.*851_*852insT	ENSP00000512448.1:n.*851_*852insT
ENST00000696159.1:c.*520_*521insT	ENSP00000512449.1:n.*520_*521insT
ENST00000696160.1:c.*9_*10insT	ENSP00000512450.1:n.*9_*10insT
ENST00000696161.1:c.727_728insT	ENSP00000512451.1:p.Arg243LeufsTer?
ENST00000696162.1:c.*1316_*1317insT	ENSP00000512452.1:n.*1316_*1317insT
ENST00000696163.1:c.*9_*10insT	ENSP00000512453.1:n.*9_*10insT
ENST00000261623.8:c.*9_*10insT MANE Select	ENSP00000261623.3:n.*9_*10insT
ENST00000261623.7:c.*9_*10insT	ENSP00000261623.3:n.*9_*10insT
NM_000101.3:c.*9_*10insT	NP_000092.2:n.*9_*10insT
NM_000101.4:c.*9_*10insT MANE Select	NP_000092.2:n.*9_*10insT