Canonical Allele Identifier: CA395951763

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56368758C>G (hg19) ; chr16:g.56334846C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56334846C>G , CM000678.2:g.56334846C>G	GRCh38
NC_000016.9:g.56368758C>G , CM000678.1:g.56368758C>G	GRCh37
NC_000016.8:g.54926259C>G	NCBI36
NG_042800.1:g.148508C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.582C>G	ENSP00000262494.7:p.Asn194Lys
ENST00000262493.12:c.582C>G MANE Select	ENSP00000262493.6:p.Asn194Lys
ENST00000262494.12:c.582C>G	ENSP00000262494.7:p.Asn194Lys
ENST00000562316.6:c.249C>G	ENSP00000457238.2:p.Asn83Lys
ENST00000638185.1:n.797C>G
ENST00000638210.1:n.882C>G
ENST00000638705.1:c.582C>G	ENSP00000491223.1:p.Asn194Lys
ENST00000638836.1:n.492C>G
ENST00000639055.1:n.1303C>G
ENST00000639251.1:n.483C>G
ENST00000639268.1:c.229-1885C>G
ENST00000639341.1:c.107C>G
ENST00000639770.1:c.620C>G	ENSP00000491999.1:n.620C>G
ENST00000640390.1:n.512C>G
ENST00000640893.1:c.421C>G	ENSP00000492677.1:p.Pro141Ala
ENST00000262493.10:c.582C>G	ENSP00000262493.6:p.Asn194Lys
ENST00000262494.11:c.582C>G	ENSP00000262494.7:p.Asn194Lys
ENST00000562316.5:c.321C>G	ENSP00000457238.1:p.Asn107Lys
NM_020988.2:c.582C>G	NP_066268.1:p.Asn194Lys
NM_138736.2:c.582C>G	NP_620073.2:p.Asn194Lys
XM_011523003.1:c.456C>G	XP_011521305.1:p.Asn152Lys
XM_011523003.3:c.456C>G	XP_011521305.1:p.Asn152Lys
NM_020988.3:c.582C>G MANE Select	NP_066268.1:p.Asn194Lys
NM_138736.3:c.582C>G	NP_620073.2:p.Asn194Lys