Canonical Allele Identifier: CA395952320

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56370724T>G (hg19) ; chr16:g.56336812T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336812T>G , CM000678.2:g.56336812T>G	GRCh38
NC_000016.9:g.56370724T>G , CM000678.1:g.56370724T>G	GRCh37
NC_000016.8:g.54928225T>G	NCBI36
NG_042800.1:g.150474T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.675T>G	ENSP00000262494.7:p.Cys225Trp
ENST00000262493.12:c.675T>G MANE Select	ENSP00000262493.6:p.Cys225Trp
ENST00000262494.12:c.675T>G	ENSP00000262494.7:p.Cys225Trp
ENST00000562316.6:c.342T>G	ENSP00000457238.2:p.Cys114Trp
ENST00000568375.2:c.67T>G
ENST00000638185.1:n.890T>G
ENST00000638210.1:n.975T>G
ENST00000638705.1:c.675T>G	ENSP00000491223.1:p.Cys225Trp
ENST00000638836.1:n.585T>G
ENST00000639055.1:n.1396T>G
ENST00000639251.1:n.576T>G
ENST00000639268.1:c.310T>G
ENST00000639341.1:c.200T>G
ENST00000639770.1:c.713T>G	ENSP00000491999.1:n.713T>G
ENST00000640390.1:n.605T>G
ENST00000640469.1:c.39T>G	ENSP00000491875.1:p.Cys13Trp
ENST00000640560.1:n.451T>G
ENST00000640893.1:c.*73T>G	ENSP00000492677.1:n.*73T>G
ENST00000262493.10:c.675T>G	ENSP00000262493.6:p.Cys225Trp
ENST00000262494.11:c.675T>G	ENSP00000262494.7:p.Cys225Trp
ENST00000568375.1:n.67T>G
NM_020988.2:c.675T>G	NP_066268.1:p.Cys225Trp
NM_138736.2:c.675T>G	NP_620073.2:p.Cys225Trp
XM_011523003.1:c.549T>G	XP_011521305.1:p.Cys183Trp
XM_011523003.3:c.549T>G	XP_011521305.1:p.Cys183Trp
NM_020988.3:c.675T>G MANE Select	NP_066268.1:p.Cys225Trp
NM_138736.3:c.675T>G	NP_620073.2:p.Cys225Trp