Canonical Allele Identifier: CA2224108732
Gene: GNAO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56351404C= , CM000678.2:g.56351404C= GRCh38
NC_000016.9:g.56385316C= , CM000678.1:g.56385316C= GRCh37
NC_000016.8:g.54942817C= NCBI36
NG_042800.1:g.165066C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262493.12:c.744C= MANE Select ENSP00000262493.6:p.Leu248=
ENST00000562316.6:c.411C= ENSP00000457238.2:p.Leu137=
ENST00000564727.2:c.48C= ENSP00000454971.2:p.Leu16=
ENST00000568375.2:c.116-3462C=
ENST00000638185.1:n.959C=
ENST00000638210.1:n.1044C=
ENST00000638705.1:c.744C= ENSP00000491223.1:p.Leu248=
ENST00000638836.1:n.654C=
ENST00000639055.1:n.1465C=
ENST00000639251.1:n.645C=
ENST00000639268.1:c.379C=
ENST00000639341.1:c.269C=
ENST00000639770.1:c.782C= ENSP00000491999.1:n.782C=
ENST00000640390.1:n.674C=
ENST00000640469.1:c.108C= ENSP00000491875.1:p.Leu36=
ENST00000640560.1:n.520C=
ENST00000640893.1:c.*142C= ENSP00000492677.1:n.*142C=
ENST00000262493.10:c.744C= ENSP00000262493.6:p.Leu248=
ENST00000568375.1:n.116-3462C=
NM_020988.2:c.744C= NP_066268.1:p.Leu248=
XM_011523003.1:c.618C= XP_011521305.1:p.Leu206=
XM_011523003.3:c.618C= XP_011521305.1:p.Leu206=
NM_020988.3:c.744C= MANE Select NP_066268.1:p.Leu248=