Canonical Allele Identifier: CA2241199539

Gene: CYBA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88643333_88643334delinsAG , CM000678.2:g.88643333_88643334delinsAG	GRCh38
NC_000016.9:g.88709741_88709742delinsAG , CM000678.1:g.88709741_88709742delinsAG	GRCh37
NC_000016.8:g.87237242_87237243delinsAG	NCBI36
NG_007291.1:g.12716_12717delinsCT , LRG_52:g.12716_12717delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000696156.1:c.*19_*20delinsCT	ENSP00000512446.1:n.*19_*20delinsCT
ENST00000696157.1:c.*824_*825delinsCT	ENSP00000512447.1:n.*824_*825delinsCT
ENST00000696158.1:c.*861_*862delinsCT	ENSP00000512448.1:n.*861_*862delinsCT
ENST00000696159.1:c.*530_*531delinsCT	ENSP00000512449.1:n.*530_*531delinsCT
ENST00000696160.1:c.*19_*20delinsCT	ENSP00000512450.1:n.*19_*20delinsCT
ENST00000696161.1:c.737_738delinsCT	ENSP00000512451.1:p.Pro246=
ENST00000696162.1:c.*1326_*1327delinsCT	ENSP00000512452.1:n.*1326_*1327delinsCT
ENST00000696163.1:c.*19_*20delinsCT	ENSP00000512453.1:n.*19_*20delinsCT
ENST00000261623.8:c.*19_*20delinsCT MANE Select	ENSP00000261623.3:n.*19_*20delinsCT
ENST00000261623.7:c.*19_*20delinsCT	ENSP00000261623.3:n.*19_*20delinsCT
NM_000101.3:c.*19_*20delinsCT	NP_000092.2:n.*19_*20delinsCT
NM_000101.4:c.*19_*20delinsCT MANE Select	NP_000092.2:n.*19_*20delinsCT