Canonical Allele Identifier: CA395954873

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56385420C>G (hg19) ; chr16:g.56351508C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351508C>G , CM000678.2:g.56351508C>G	GRCh38
NC_000016.9:g.56385420C>G , CM000678.1:g.56385420C>G	GRCh37
NC_000016.8:g.54942921C>G	NCBI36
NG_042800.1:g.165170C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.848C>G MANE Select	ENSP00000262493.6:p.Pro283Arg
ENST00000562316.6:c.515C>G	ENSP00000457238.2:p.Pro172Arg
ENST00000564727.2:c.152C>G	ENSP00000454971.2:p.Pro51Arg
ENST00000568375.2:c.116-3358C>G
ENST00000638185.1:n.1063C>G
ENST00000638210.1:n.1148C>G
ENST00000638705.1:c.848C>G	ENSP00000491223.1:p.Pro283Arg
ENST00000638836.1:n.758C>G
ENST00000639055.1:n.1569C>G
ENST00000639251.1:n.749C>G
ENST00000639268.1:c.483C>G
ENST00000639341.1:c.373C>G
ENST00000639770.1:c.886C>G	ENSP00000491999.1:n.886C>G
ENST00000640390.1:n.778C>G
ENST00000640469.1:c.212C>G	ENSP00000491875.1:p.Pro71Arg
ENST00000640560.1:n.624C>G
ENST00000640893.1:c.*246C>G	ENSP00000492677.1:n.*246C>G
ENST00000262493.10:c.848C>G	ENSP00000262493.6:p.Pro283Arg
ENST00000564727.1:c.68C>G	ENSP00000454971.1:p.Pro23Arg
ENST00000568375.1:n.116-3358C>G
NM_020988.2:c.848C>G	NP_066268.1:p.Pro283Arg
XM_011523003.1:c.722C>G	XP_011521305.1:p.Pro241Arg
XM_011523003.3:c.722C>G	XP_011521305.1:p.Pro241Arg
NM_020988.3:c.848C>G MANE Select	NP_066268.1:p.Pro283Arg