Canonical Allele Identifier: CA624448019

Gene: CYBA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88643589del , CM000678.2:g.88643589del	GRCh38
NC_000016.9:g.88709997del , CM000678.1:g.88709997del	GRCh37
NC_000016.8:g.87237498del	NCBI36
NG_007291.1:g.12463del , LRG_52:g.12463del

Transcript Alleles

HGVS	Amino-acid Change
NM_000101.4:c.370-16del MANE Select	NP_000092.2:n.370-16del
ENST00000261623.8:c.370-16del MANE Select	ENSP00000261623.3:n.370-16del
NM_000101.3:c.370-16del	NP_000092.2:n.370-16del
ENST00000261623.7:c.370-16del	ENSP00000261623.3:n.370-16del
ENST00000565588.5:c.154-6del
ENST00000565588.6:c.370-6del	ENSP00000455537.2:n.370-6del
ENST00000566229.1:c.359-16del	ENSP00000457060.1:n.359-16del
ENST00000566534.5:n.949-16del
ENST00000696156.1:c.286-16del	ENSP00000512446.1:n.286-16del
ENST00000696157.1:c.*571del	ENSP00000512447.1:n.*571del
ENST00000696158.1:c.*608del	ENSP00000512448.1:n.*608del
ENST00000696159.1:c.*277del	ENSP00000512449.1:n.*277del
ENST00000696160.1:c.397-16del	ENSP00000512450.1:n.397-16del
ENST00000696161.1:c.500-16del	ENSP00000512451.1:n.500-16del
ENST00000696162.1:c.*1073del	ENSP00000512452.1:n.*1073del
ENST00000696163.1:c.319-16del	ENSP00000512453.1:n.319-16del
XM_011522905.3:c.*1579del	XP_011521207.1:n.*1579del