Canonical Allele Identifier: CA395951378

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56368644C>G (hg19) ; chr16:g.56334732C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.468C>G	ENSP00000262494.7:p.Tyr156Ter
ENST00000262493.12:c.468C>G MANE Select	ENSP00000262493.6:p.Tyr156Ter
ENST00000262494.12:c.468C>G	ENSP00000262494.7:p.Tyr156Ter
ENST00000562316.6:c.135C>G	ENSP00000457238.2:p.Tyr45Ter
ENST00000638185.1:n.683C>G
ENST00000638210.1:n.768C>G
ENST00000638705.1:c.468C>G	ENSP00000491223.1:p.Tyr156Ter
ENST00000638836.1:n.378C>G
ENST00000639055.1:n.1189C>G
ENST00000639251.1:n.369C>G
ENST00000639268.1:c.229-1999C>G
ENST00000639770.1:c.506C>G	ENSP00000491999.1:n.506C>G
ENST00000640390.1:n.398C>G
ENST00000640893.1:c.307C>G	ENSP00000492677.1:p.Pro103Ala
ENST00000262493.10:c.468C>G	ENSP00000262493.6:p.Tyr156Ter
ENST00000262494.11:c.468C>G	ENSP00000262494.7:p.Tyr156Ter
ENST00000562316.5:c.207C>G	ENSP00000457238.1:p.Tyr69Ter
ENST00000563440.1:c.207C>G	ENSP00000455774.1:p.Tyr69Ter
ENST00000565363.5:c.342C>G	ENSP00000454728.1:p.Tyr114Ter
NM_020988.2:c.468C>G	NP_066268.1:p.Tyr156Ter
NM_138736.2:c.468C>G	NP_620073.2:p.Tyr156Ter
XM_011523003.1:c.342C>G	XP_011521305.1:p.Tyr114Ter
XM_011523003.3:c.342C>G	XP_011521305.1:p.Tyr114Ter
NM_020988.3:c.468C>G MANE Select	NP_066268.1:p.Tyr156Ter
NM_138736.3:c.468C>G	NP_620073.2:p.Tyr156Ter