Canonical Allele Identifier: CA2634847697

Gene: CYBA

Linked Data

• gnomAD v4: 16-88643316-TGGGTGCACCTGGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88643320_88643332del , CM000678.2:g.88643320_88643332del	GRCh38
NC_000016.9:g.88709728_88709740del , CM000678.1:g.88709728_88709740del	GRCh37
NC_000016.8:g.87237229_87237241del	NCBI36
NG_007291.1:g.12721_12733del , LRG_52:g.12721_12733del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696156.1:c.*24_*36del	ENSP00000512446.1:n.*24_*36del
ENST00000696157.1:c.*829_*841del	ENSP00000512447.1:n.*829_*841del
ENST00000696158.1:c.*866_*878del	ENSP00000512448.1:n.*866_*878del
ENST00000696159.1:c.*535_*547del	ENSP00000512449.1:n.*535_*547del
ENST00000696160.1:c.*24_*36del	ENSP00000512450.1:n.*24_*36del
ENST00000696161.1:c.742_754del	ENSP00000512451.1:p.Ala248ThrfsTer?
ENST00000696162.1:c.*1331_*1343del	ENSP00000512452.1:n.*1331_*1343del
ENST00000696163.1:c.*24_*36del	ENSP00000512453.1:n.*24_*36del
ENST00000261623.8:c.*24_*36del MANE Select	ENSP00000261623.3:n.*24_*36del
ENST00000261623.7:c.*24_*36del	ENSP00000261623.3:n.*24_*36del
NM_000101.3:c.*24_*36del	NP_000092.2:n.*24_*36del
NM_000101.4:c.*24_*36del MANE Select	NP_000092.2:n.*24_*36del