Canonical Allele Identifier: CA395954738

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56385363C>G (hg19) ; chr16:g.56351451C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351451C>G , CM000678.2:g.56351451C>G	GRCh38
NC_000016.9:g.56385363C>G , CM000678.1:g.56385363C>G	GRCh37
NC_000016.8:g.54942864C>G	NCBI36
NG_042800.1:g.165113C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.791C>G MANE Select	ENSP00000262493.6:p.Ser264Cys
ENST00000562316.6:c.458C>G	ENSP00000457238.2:p.Ser153Cys
ENST00000564727.2:c.95C>G	ENSP00000454971.2:p.Ser32Cys
ENST00000568375.2:c.116-3415C>G
ENST00000638185.1:n.1006C>G
ENST00000638210.1:n.1091C>G
ENST00000638705.1:c.791C>G	ENSP00000491223.1:p.Ser264Cys
ENST00000638836.1:n.701C>G
ENST00000639055.1:n.1512C>G
ENST00000639251.1:n.692C>G
ENST00000639268.1:c.426C>G
ENST00000639341.1:c.316C>G
ENST00000639770.1:c.829C>G	ENSP00000491999.1:n.829C>G
ENST00000640390.1:n.721C>G
ENST00000640469.1:c.155C>G	ENSP00000491875.1:p.Ser52Cys
ENST00000640560.1:n.567C>G
ENST00000640893.1:c.*189C>G	ENSP00000492677.1:n.*189C>G
ENST00000262493.10:c.791C>G	ENSP00000262493.6:p.Ser264Cys
ENST00000564727.1:c.11C>G	ENSP00000454971.1:p.Ser4Cys
ENST00000568375.1:n.116-3415C>G
NM_020988.2:c.791C>G	NP_066268.1:p.Ser264Cys
XM_011523003.1:c.665C>G	XP_011521305.1:p.Ser222Cys
XM_011523003.3:c.665C>G	XP_011521305.1:p.Ser222Cys
NM_020988.3:c.791C>G MANE Select	NP_066268.1:p.Ser264Cys