Canonical Allele Identifier: CA395952303

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56370717T>G (hg19) ; chr16:g.56336805T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336805T>G , CM000678.2:g.56336805T>G	GRCh38
NC_000016.9:g.56370717T>G , CM000678.1:g.56370717T>G	GRCh37
NC_000016.8:g.54928218T>G	NCBI36
NG_042800.1:g.150467T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.668T>G	ENSP00000262494.7:p.Ile223Ser
ENST00000262493.12:c.668T>G MANE Select	ENSP00000262493.6:p.Ile223Ser
ENST00000262494.12:c.668T>G	ENSP00000262494.7:p.Ile223Ser
ENST00000562316.6:c.335T>G	ENSP00000457238.2:p.Ile112Ser
ENST00000568375.2:c.60T>G
ENST00000638185.1:n.883T>G
ENST00000638210.1:n.968T>G
ENST00000638705.1:c.668T>G	ENSP00000491223.1:p.Ile223Ser
ENST00000638836.1:n.578T>G
ENST00000639055.1:n.1389T>G
ENST00000639251.1:n.569T>G
ENST00000639268.1:c.303T>G
ENST00000639341.1:c.193T>G
ENST00000639770.1:c.706T>G	ENSP00000491999.1:n.706T>G
ENST00000640390.1:n.598T>G
ENST00000640469.1:c.32T>G	ENSP00000491875.1:p.Ile11Ser
ENST00000640560.1:n.444T>G
ENST00000640893.1:c.*66T>G	ENSP00000492677.1:n.*66T>G
ENST00000262493.10:c.668T>G	ENSP00000262493.6:p.Ile223Ser
ENST00000262494.11:c.668T>G	ENSP00000262494.7:p.Ile223Ser
ENST00000568375.1:n.60T>G
NM_020988.2:c.668T>G	NP_066268.1:p.Ile223Ser
NM_138736.2:c.668T>G	NP_620073.2:p.Ile223Ser
XM_011523003.1:c.542T>G	XP_011521305.1:p.Ile181Ser
XM_011523003.3:c.542T>G	XP_011521305.1:p.Ile181Ser
NM_020988.3:c.668T>G MANE Select	NP_066268.1:p.Ile223Ser
NM_138736.3:c.668T>G	NP_620073.2:p.Ile223Ser