Canonical Allele Identifier: CA395955014

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56388807T>C (hg19) ; chr16:g.56354895T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56354895T>C , CM000678.2:g.56354895T>C	GRCh38
NC_000016.9:g.56388807T>C , CM000678.1:g.56388807T>C	GRCh37
NC_000016.8:g.54946308T>C	NCBI36
NG_042800.1:g.168557T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.907T>C MANE Select	ENSP00000262493.6:p.Tyr303His
ENST00000562316.6:c.545-1208T>C	ENSP00000457238.2:n.545-1208T>C
ENST00000564727.2:c.211T>C	ENSP00000454971.2:p.Tyr71His
ENST00000568375.2:c.145T>C
ENST00000638185.1:n.1122T>C
ENST00000638210.1:n.1207T>C
ENST00000638705.1:c.907T>C	ENSP00000491223.1:p.Tyr303His
ENST00000638836.1:n.817T>C
ENST00000639055.1:n.1628T>C
ENST00000639251.1:n.808T>C
ENST00000639268.1:c.542T>C
ENST00000639341.1:c.432T>C
ENST00000639770.1:c.945T>C	ENSP00000491999.1:n.945T>C
ENST00000640390.1:n.837T>C
ENST00000640469.1:c.271T>C	ENSP00000491875.1:p.Tyr91His
ENST00000640560.1:n.683T>C
ENST00000640893.1:c.*305T>C	ENSP00000492677.1:n.*305T>C
ENST00000262493.10:c.907T>C	ENSP00000262493.6:p.Tyr303His
ENST00000564727.1:c.127T>C	ENSP00000454971.1:p.Tyr43His
ENST00000568375.1:n.145T>C
NM_020988.2:c.907T>C	NP_066268.1:p.Tyr303His
XM_011523003.1:c.781T>C	XP_011521305.1:p.Tyr261His
XM_011523003.3:c.781T>C	XP_011521305.1:p.Tyr261His
NM_020988.3:c.907T>C MANE Select	NP_066268.1:p.Tyr303His