Canonical Allele Identifier: CA2241201851
Gene: CYBA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88647111_88647112delinsTG , CM000678.2:g.88647111_88647112delinsTG GRCh38
NC_000016.9:g.88713519_88713520delinsTG , CM000678.1:g.88713519_88713520delinsTG GRCh37
NC_000016.8:g.87241020_87241021delinsTG NCBI36
NG_007291.1:g.8938_8939delinsCA , LRG_52:g.8938_8939delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000565588.6:c.192_193delinsCA ENSP00000455537.2:p.Thr64=
ENST00000696156.1:c.192_193delinsCA ENSP00000512446.1:p.Thr64=
ENST00000696157.1:c.192_193delinsCA ENSP00000512447.1:p.Thr64=
ENST00000696158.1:c.192_193delinsCA ENSP00000512448.1:p.Thr64=
ENST00000696159.1:c.192_193delinsCA ENSP00000512449.1:p.Thr64=
ENST00000696160.1:c.192_193delinsCA ENSP00000512450.1:p.Thr64=
ENST00000696161.1:c.192_193delinsCA ENSP00000512451.1:p.Thr64=
ENST00000696162.1:c.192_193delinsCA ENSP00000512452.1:p.Thr64=
ENST00000696163.1:c.192_193delinsCA ENSP00000512453.1:p.Thr64=
ENST00000261623.8:c.192_193delinsCA MANE Select ENSP00000261623.3:p.Thr64=
ENST00000261623.7:c.192_193delinsCA ENSP00000261623.3:p.Thr64=
ENST00000562209.1:n.210_211delinsCA
ENST00000563526.5:n.167_168delinsCA
ENST00000566229.1:c.181_182delinsCA ENSP00000457060.1:p.His61=
ENST00000566534.5:n.214_215delinsCA
ENST00000567174.5:c.192_193delinsCA ENSP00000454951.1:p.Thr64=
ENST00000568278.1:c.192_193delinsCA ENSP00000455506.1:p.Thr64=
ENST00000569359.5:c.192_193delinsCA ENSP00000456079.1:p.Thr64=
NM_000101.3:c.192_193delinsCA NP_000092.2:p.Thr64=
XM_011522905.1:c.192_193delinsCA XP_011521207.1:p.Thr64=
XM_011522905.3:c.192_193delinsCA XP_011521207.1:p.Thr64=
NM_000101.4:c.192_193delinsCA MANE Select NP_000092.2:p.Thr64=