Canonical Allele Identifier: CA395951369
Gene: GNAO1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56334729C>G , CM000678.2:g.56334729C>G GRCh38
NC_000016.9:g.56368641C>G , CM000678.1:g.56368641C>G GRCh37
NC_000016.8:g.54926142C>G NCBI36
NG_042800.1:g.148391C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262494.13:c.465C>G ENSP00000262494.7:p.Tyr155Ter
ENST00000262493.12:c.465C>G MANE Select ENSP00000262493.6:p.Tyr155Ter
ENST00000262494.12:c.465C>G ENSP00000262494.7:p.Tyr155Ter
ENST00000562316.6:c.132C>G ENSP00000457238.2:p.Tyr44Ter
ENST00000638185.1:n.680C>G
ENST00000638210.1:n.765C>G
ENST00000638705.1:c.465C>G ENSP00000491223.1:p.Tyr155Ter
ENST00000638836.1:n.375C>G
ENST00000639055.1:n.1186C>G
ENST00000639251.1:n.366C>G
ENST00000639268.1:c.229-2002C>G
ENST00000639770.1:c.503C>G ENSP00000491999.1:n.503C>G
ENST00000640390.1:n.395C>G
ENST00000640893.1:c.304C>G ENSP00000492677.1:p.Leu102Val
ENST00000262493.10:c.465C>G ENSP00000262493.6:p.Tyr155Ter
ENST00000262494.11:c.465C>G ENSP00000262494.7:p.Tyr155Ter
ENST00000562316.5:c.204C>G ENSP00000457238.1:p.Tyr68Ter
ENST00000563440.1:c.204C>G ENSP00000455774.1:p.Tyr68Ter
ENST00000565363.5:c.339C>G ENSP00000454728.1:p.Tyr113Ter
NM_020988.2:c.465C>G NP_066268.1:p.Tyr155Ter
NM_138736.2:c.465C>G NP_620073.2:p.Tyr155Ter
XM_011523003.1:c.339C>G XP_011521305.1:p.Tyr113Ter
XM_011523003.3:c.339C>G XP_011521305.1:p.Tyr113Ter
NM_020988.3:c.465C>G MANE Select NP_066268.1:p.Tyr155Ter
NM_138736.3:c.465C>G NP_620073.2:p.Tyr155Ter