Canonical Allele Identifier: CA395951377
Gene: GNAO1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56334732C>A , CM000678.2:g.56334732C>A GRCh38
NC_000016.9:g.56368644C>A , CM000678.1:g.56368644C>A GRCh37
NC_000016.8:g.54926145C>A NCBI36
NG_042800.1:g.148394C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262494.13:c.468C>A ENSP00000262494.7:p.Tyr156Ter
ENST00000262493.12:c.468C>A MANE Select ENSP00000262493.6:p.Tyr156Ter
ENST00000262494.12:c.468C>A ENSP00000262494.7:p.Tyr156Ter
ENST00000562316.6:c.135C>A ENSP00000457238.2:p.Tyr45Ter
ENST00000638185.1:n.683C>A
ENST00000638210.1:n.768C>A
ENST00000638705.1:c.468C>A ENSP00000491223.1:p.Tyr156Ter
ENST00000638836.1:n.378C>A
ENST00000639055.1:n.1189C>A
ENST00000639251.1:n.369C>A
ENST00000639268.1:c.229-1999C>A
ENST00000639770.1:c.506C>A ENSP00000491999.1:n.506C>A
ENST00000640390.1:n.398C>A
ENST00000640893.1:c.307C>A ENSP00000492677.1:p.Pro103Thr
ENST00000262493.10:c.468C>A ENSP00000262493.6:p.Tyr156Ter
ENST00000262494.11:c.468C>A ENSP00000262494.7:p.Tyr156Ter
ENST00000562316.5:c.207C>A ENSP00000457238.1:p.Tyr69Ter
ENST00000563440.1:c.207C>A ENSP00000455774.1:p.Tyr69Ter
ENST00000565363.5:c.342C>A ENSP00000454728.1:p.Tyr114Ter
NM_020988.2:c.468C>A NP_066268.1:p.Tyr156Ter
NM_138736.2:c.468C>A NP_620073.2:p.Tyr156Ter
XM_011523003.1:c.342C>A XP_011521305.1:p.Tyr114Ter
XM_011523003.3:c.342C>A XP_011521305.1:p.Tyr114Ter
NM_020988.3:c.468C>A MANE Select NP_066268.1:p.Tyr156Ter
NM_138736.3:c.468C>A NP_620073.2:p.Tyr156Ter