Canonical Allele Identifier: CA395954746

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56385367C>G (hg19) ; chr16:g.56351455C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351455C>G , CM000678.2:g.56351455C>G	GRCh38
NC_000016.9:g.56385367C>G , CM000678.1:g.56385367C>G	GRCh37
NC_000016.8:g.54942868C>G	NCBI36
NG_042800.1:g.165117C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.795C>G MANE Select	ENSP00000262493.6:p.Ile265Met
ENST00000562316.6:c.462C>G	ENSP00000457238.2:p.Ile154Met
ENST00000564727.2:c.99C>G	ENSP00000454971.2:p.Ile33Met
ENST00000568375.2:c.116-3411C>G
ENST00000638185.1:n.1010C>G
ENST00000638210.1:n.1095C>G
ENST00000638705.1:c.795C>G	ENSP00000491223.1:p.Ile265Met
ENST00000638836.1:n.705C>G
ENST00000639055.1:n.1516C>G
ENST00000639251.1:n.696C>G
ENST00000639268.1:c.430C>G
ENST00000639341.1:c.320C>G
ENST00000639770.1:c.833C>G	ENSP00000491999.1:n.833C>G
ENST00000640390.1:n.725C>G
ENST00000640469.1:c.159C>G	ENSP00000491875.1:p.Ile53Met
ENST00000640560.1:n.571C>G
ENST00000640893.1:c.*193C>G	ENSP00000492677.1:n.*193C>G
ENST00000262493.10:c.795C>G	ENSP00000262493.6:p.Ile265Met
ENST00000564727.1:c.15C>G	ENSP00000454971.1:p.Ile5Met
ENST00000568375.1:n.116-3411C>G
NM_020988.2:c.795C>G	NP_066268.1:p.Ile265Met
XM_011523003.1:c.669C>G	XP_011521305.1:p.Ile223Met
XM_011523003.3:c.669C>G	XP_011521305.1:p.Ile223Met
NM_020988.3:c.795C>G MANE Select	NP_066268.1:p.Ile265Met