Canonical Allele Identifier: CA395954957

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56388781C>G (hg19) ; chr16:g.56354869C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56354869C>G , CM000678.2:g.56354869C>G	GRCh38
NC_000016.9:g.56388781C>G , CM000678.1:g.56388781C>G	GRCh37
NC_000016.8:g.54946282C>G	NCBI36
NG_042800.1:g.168531C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.881C>G MANE Select	ENSP00000262493.6:p.Pro294Arg
ENST00000562316.6:c.545-1234C>G	ENSP00000457238.2:n.545-1234C>G
ENST00000564727.2:c.185C>G	ENSP00000454971.2:p.Pro62Arg
ENST00000568375.2:c.119C>G
ENST00000638185.1:n.1096C>G
ENST00000638210.1:n.1181C>G
ENST00000638705.1:c.881C>G	ENSP00000491223.1:p.Pro294Arg
ENST00000638836.1:n.791C>G
ENST00000639055.1:n.1602C>G
ENST00000639251.1:n.782C>G
ENST00000639268.1:c.516C>G
ENST00000639341.1:c.406C>G
ENST00000639770.1:c.919C>G	ENSP00000491999.1:n.919C>G
ENST00000640390.1:n.811C>G
ENST00000640469.1:c.245C>G	ENSP00000491875.1:p.Pro82Arg
ENST00000640560.1:n.657C>G
ENST00000640893.1:c.*279C>G	ENSP00000492677.1:n.*279C>G
ENST00000262493.10:c.881C>G	ENSP00000262493.6:p.Pro294Arg
ENST00000564727.1:c.101C>G	ENSP00000454971.1:p.Pro34Arg
ENST00000568375.1:n.119C>G
NM_020988.2:c.881C>G	NP_066268.1:p.Pro294Arg
XM_011523003.1:c.755C>G	XP_011521305.1:p.Pro252Arg
XM_011523003.3:c.755C>G	XP_011521305.1:p.Pro252Arg
NM_020988.3:c.881C>G MANE Select	NP_066268.1:p.Pro294Arg