Canonical Allele Identifier: CA495573653

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56370742T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336830T>C , CM000678.2:g.56336830T>C	GRCh38
NC_000016.9:g.56370742T>C , CM000678.1:g.56370742T>C	GRCh37
NC_000016.8:g.54928243T>C	NCBI36
NG_042800.1:g.150492T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000262494.13:c.693T>C	ENSP00000262494.7:p.Tyr231=
ENST00000262493.12:c.693T>C MANE Select	ENSP00000262493.6:p.Tyr231=
ENST00000262494.12:c.693T>C	ENSP00000262494.7:p.Tyr231=
ENST00000562316.6:c.360T>C	ENSP00000457238.2:p.Tyr120=
ENST00000568375.2:c.85T>C
ENST00000638185.1:n.908T>C
ENST00000638210.1:n.993T>C
ENST00000638705.1:c.693T>C	ENSP00000491223.1:p.Tyr231=
ENST00000638836.1:n.603T>C
ENST00000639055.1:n.1414T>C
ENST00000639251.1:n.594T>C
ENST00000639268.1:c.328T>C
ENST00000639341.1:c.218T>C
ENST00000639770.1:c.731T>C	ENSP00000491999.1:n.731T>C
ENST00000640390.1:n.623T>C
ENST00000640469.1:c.57T>C	ENSP00000491875.1:p.Tyr19=
ENST00000640560.1:n.469T>C
ENST00000640893.1:c.*91T>C	ENSP00000492677.1:n.*91T>C
ENST00000262493.10:c.693T>C	ENSP00000262493.6:p.Tyr231=
ENST00000262494.11:c.693T>C	ENSP00000262494.7:p.Tyr231=
ENST00000568375.1:n.85T>C
NM_020988.2:c.693T>C	NP_066268.1:p.Tyr231=
NM_138736.2:c.693T>C	NP_620073.2:p.Tyr231=
XM_011523003.1:c.567T>C	XP_011521305.1:p.Tyr189=
XM_011523003.3:c.567T>C	XP_011521305.1:p.Tyr189=
NM_020988.3:c.693T>C MANE Select	NP_066268.1:p.Tyr231=
NM_138736.3:c.693T>C	NP_620073.2:p.Tyr231=