Canonical Allele Identifier: CA495573435

Gene: GNAO1

Linked Data

• gnomAD v4: 16-56334729-C-T
• MyVariant Identifiers: chr16:g.56368641C>T (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.465C>T	ENSP00000262494.7:p.Tyr155=
ENST00000262493.12:c.465C>T MANE Select	ENSP00000262493.6:p.Tyr155=
ENST00000262494.12:c.465C>T	ENSP00000262494.7:p.Tyr155=
ENST00000562316.6:c.132C>T	ENSP00000457238.2:p.Tyr44=
ENST00000638185.1:n.680C>T
ENST00000638210.1:n.765C>T
ENST00000638705.1:c.465C>T	ENSP00000491223.1:p.Tyr155=
ENST00000638836.1:n.375C>T
ENST00000639055.1:n.1186C>T
ENST00000639251.1:n.366C>T
ENST00000639268.1:c.229-2002C>T
ENST00000639770.1:c.503C>T	ENSP00000491999.1:n.503C>T
ENST00000640390.1:n.395C>T
ENST00000640893.1:c.304C>T	ENSP00000492677.1:p.Leu102=
ENST00000262493.10:c.465C>T	ENSP00000262493.6:p.Tyr155=
ENST00000262494.11:c.465C>T	ENSP00000262494.7:p.Tyr155=
ENST00000562316.5:c.204C>T	ENSP00000457238.1:p.Tyr68=
ENST00000563440.1:c.204C>T	ENSP00000455774.1:p.Tyr68=
ENST00000565363.5:c.339C>T	ENSP00000454728.1:p.Tyr113=
NM_020988.2:c.465C>T	NP_066268.1:p.Tyr155=
NM_138736.2:c.465C>T	NP_620073.2:p.Tyr155=
XM_011523003.1:c.339C>T	XP_011521305.1:p.Tyr113=
XM_011523003.3:c.339C>T	XP_011521305.1:p.Tyr113=
NM_020988.3:c.465C>T MANE Select	NP_066268.1:p.Tyr155=
NM_138736.3:c.465C>T	NP_620073.2:p.Tyr155=