Canonical Allele Identifier: CA2224108726
Gene: GNAO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56351385A= , CM000678.2:g.56351385A= GRCh38
NC_000016.9:g.56385297A= , CM000678.1:g.56385297A= GRCh37
NC_000016.8:g.54942798A= NCBI36
NG_042800.1:g.165047A=

Transcript Alleles

HGVS Amino-acid change
ENST00000262493.12:c.725A= MANE Select ENSP00000262493.6:p.Asn242=
ENST00000562316.6:c.392A= ENSP00000457238.2:p.Asn131=
ENST00000564727.2:c.29A= ENSP00000454971.2:p.Asn10=
ENST00000568375.2:c.116-3481A=
ENST00000638185.1:n.940A=
ENST00000638210.1:n.1025A=
ENST00000638705.1:c.725A= ENSP00000491223.1:p.Asn242=
ENST00000638836.1:n.635A=
ENST00000639055.1:n.1446A=
ENST00000639251.1:n.626A=
ENST00000639268.1:c.360A=
ENST00000639341.1:c.250A=
ENST00000639770.1:c.763A= ENSP00000491999.1:n.763A=
ENST00000640390.1:n.655A=
ENST00000640469.1:c.89A= ENSP00000491875.1:p.Asn30=
ENST00000640560.1:n.501A=
ENST00000640893.1:c.*123A= ENSP00000492677.1:n.*123A=
ENST00000262493.10:c.725A= ENSP00000262493.6:p.Asn242=
ENST00000568375.1:n.116-3481A=
NM_020988.2:c.725A= NP_066268.1:p.Asn242=
XM_011523003.1:c.599A= XP_011521305.1:p.Asn200=
XM_011523003.3:c.599A= XP_011521305.1:p.Asn200=
NM_020988.3:c.725A= MANE Select NP_066268.1:p.Asn242=