Canonical Allele Identifier: CA395954752

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56385369T>G (hg19) ; chr16:g.56351457T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351457T>G , CM000678.2:g.56351457T>G	GRCh38
NC_000016.9:g.56385369T>G , CM000678.1:g.56385369T>G	GRCh37
NC_000016.8:g.54942870T>G	NCBI36
NG_042800.1:g.165119T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.797T>G MANE Select	ENSP00000262493.6:p.Ile266Ser
ENST00000562316.6:c.464T>G	ENSP00000457238.2:p.Ile155Ser
ENST00000564727.2:c.101T>G	ENSP00000454971.2:p.Ile34Ser
ENST00000568375.2:c.116-3409T>G
ENST00000638185.1:n.1012T>G
ENST00000638210.1:n.1097T>G
ENST00000638705.1:c.797T>G	ENSP00000491223.1:p.Ile266Ser
ENST00000638836.1:n.707T>G
ENST00000639055.1:n.1518T>G
ENST00000639251.1:n.698T>G
ENST00000639268.1:c.432T>G
ENST00000639341.1:c.322T>G
ENST00000639770.1:c.835T>G	ENSP00000491999.1:n.835T>G
ENST00000640390.1:n.727T>G
ENST00000640469.1:c.161T>G	ENSP00000491875.1:p.Ile54Ser
ENST00000640560.1:n.573T>G
ENST00000640893.1:c.*195T>G	ENSP00000492677.1:n.*195T>G
ENST00000262493.10:c.797T>G	ENSP00000262493.6:p.Ile266Ser
ENST00000564727.1:c.17T>G	ENSP00000454971.1:p.Ile6Ser
ENST00000568375.1:n.116-3409T>G
NM_020988.2:c.797T>G	NP_066268.1:p.Ile266Ser
XM_011523003.1:c.671T>G	XP_011521305.1:p.Ile224Ser
XM_011523003.3:c.671T>G	XP_011521305.1:p.Ile224Ser
NM_020988.3:c.797T>G MANE Select	NP_066268.1:p.Ile266Ser