Canonical Allele Identifier: CA2634847721

Gene: CYBA

Linked Data

• gnomAD v4: 16-88643331-GGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88643333_88643334del , CM000678.2:g.88643333_88643334del	GRCh38
NC_000016.9:g.88709741_88709742del , CM000678.1:g.88709741_88709742del	GRCh37
NC_000016.8:g.87237242_87237243del	NCBI36
NG_007291.1:g.12717_12718del , LRG_52:g.12717_12718del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696156.1:c.*20_*21del	ENSP00000512446.1:n.*20_*21del
ENST00000696157.1:c.*825_*826del	ENSP00000512447.1:n.*825_*826del
ENST00000696158.1:c.*862_*863del	ENSP00000512448.1:n.*862_*863del
ENST00000696159.1:c.*531_*532del	ENSP00000512449.1:n.*531_*532del
ENST00000696160.1:c.*20_*21del	ENSP00000512450.1:n.*20_*21del
ENST00000696161.1:c.738_739del	ENSP00000512451.1:p.Pro247ArgfsTer?
ENST00000696162.1:c.*1327_*1328del	ENSP00000512452.1:n.*1327_*1328del
ENST00000696163.1:c.*20_*21del	ENSP00000512453.1:n.*20_*21del
ENST00000261623.8:c.*20_*21del MANE Select	ENSP00000261623.3:n.*20_*21del
ENST00000261623.7:c.*20_*21del	ENSP00000261623.3:n.*20_*21del
NM_000101.3:c.*20_*21del	NP_000092.2:n.*20_*21del
NM_000101.4:c.*20_*21del MANE Select	NP_000092.2:n.*20_*21del