Canonical Allele Identifier: CA2241201834

Gene: CYBA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88647086_88647092delinsCAGGAGG , CM000678.2:g.88647086_88647092delinsCAGGAGG	GRCh38
NC_000016.9:g.88713494_88713500delinsCAGGAGG , CM000678.1:g.88713494_88713500delinsCAGGAGG	GRCh37
NC_000016.8:g.87240995_87241001delinsCAGGAGG	NCBI36
NG_007291.1:g.8958_8964delinsCCTCCTG , LRG_52:g.8958_8964delinsCCTCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000565588.6:c.203+9_203+15delinsCCTCCTG	ENSP00000455537.2:n.203+9_203+15delinsCCTCCTG
ENST00000696156.1:c.203+9_203+15delinsCCTCCTG	ENSP00000512446.1:n.203+9_203+15delinsCCTCCTG
ENST00000696157.1:c.203+9_203+15delinsCCTCCTG	ENSP00000512447.1:n.203+9_203+15delinsCCTCCTG
ENST00000696158.1:c.203+9_203+15delinsCCTCCTG	ENSP00000512448.1:n.203+9_203+15delinsCCTCCTG
ENST00000696159.1:c.203+9_203+15delinsCCTCCTG	ENSP00000512449.1:n.203+9_203+15delinsCCTCCTG
ENST00000696160.1:c.203+9_203+15delinsCCTCCTG	ENSP00000512450.1:n.203+9_203+15delinsCCTCCTG
ENST00000696161.1:c.203+9_203+15delinsCCTCCTG	ENSP00000512451.1:n.203+9_203+15delinsCCTCCTG
ENST00000696162.1:c.203+9_203+15delinsCCTCCTG	ENSP00000512452.1:n.203+9_203+15delinsCCTCCTG
ENST00000696163.1:c.203+9_203+15delinsCCTCCTG	ENSP00000512453.1:n.203+9_203+15delinsCCTCCTG
ENST00000261623.8:c.203+9_203+15delinsCCTCCTG MANE Select	ENSP00000261623.3:n.203+9_203+15delinsCCTCCTG
ENST00000261623.7:c.203+9_203+15delinsCCTCCTG	ENSP00000261623.3:n.203+9_203+15delinsCCTCCTG
ENST00000562209.1:n.230_236delinsCCTCCTG
ENST00000563526.5:n.178+9_178+15delinsCCTCCTG
ENST00000566229.1:c.192+9_192+15delinsCCTCCTG	ENSP00000457060.1:n.192+9_192+15delinsCCTCCTG
ENST00000566534.5:n.225+9_225+15delinsCCTCCTG
ENST00000567174.5:c.203+9_203+15delinsCCTCCTG	ENSP00000454951.1:n.203+9_203+15delinsCCTCCTG
ENST00000568278.1:c.203+9_203+15delinsCCTCCTG	ENSP00000455506.1:n.203+9_203+15delinsCCTCCTG
ENST00000569359.5:c.203+9_203+15delinsCCTCCTG	ENSP00000456079.1:n.203+9_203+15delinsCCTCCTG
NM_000101.3:c.203+9_203+15delinsCCTCCTG	NP_000092.2:n.203+9_203+15delinsCCTCCTG
XM_011522905.1:c.203+9_203+15delinsCCTCCTG	XP_011521207.1:n.203+9_203+15delinsCCTCCTG
XM_011522905.3:c.203+9_203+15delinsCCTCCTG	XP_011521207.1:n.203+9_203+15delinsCCTCCTG
NM_000101.4:c.203+9_203+15delinsCCTCCTG MANE Select	NP_000092.2:n.203+9_203+15delinsCCTCCTG