Canonical Allele Identifier: CA395955009

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56388804G>T (hg19) ; chr16:g.56354892G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56354892G>T , CM000678.2:g.56354892G>T	GRCh38
NC_000016.9:g.56388804G>T , CM000678.1:g.56388804G>T	GRCh37
NC_000016.8:g.54946305G>T	NCBI36
NG_042800.1:g.168554G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.904G>T MANE Select	ENSP00000262493.6:p.Ala302Ser
ENST00000562316.6:c.545-1211G>T	ENSP00000457238.2:n.545-1211G>T
ENST00000564727.2:c.208G>T	ENSP00000454971.2:p.Ala70Ser
ENST00000568375.2:c.142G>T
ENST00000638185.1:n.1119G>T
ENST00000638210.1:n.1204G>T
ENST00000638705.1:c.904G>T	ENSP00000491223.1:p.Ala302Ser
ENST00000638836.1:n.814G>T
ENST00000639055.1:n.1625G>T
ENST00000639251.1:n.805G>T
ENST00000639268.1:c.539G>T
ENST00000639341.1:c.429G>T
ENST00000639770.1:c.942G>T	ENSP00000491999.1:n.942G>T
ENST00000640390.1:n.834G>T
ENST00000640469.1:c.268G>T	ENSP00000491875.1:p.Ala90Ser
ENST00000640560.1:n.680G>T
ENST00000640893.1:c.*302G>T	ENSP00000492677.1:n.*302G>T
ENST00000262493.10:c.904G>T	ENSP00000262493.6:p.Ala302Ser
ENST00000564727.1:c.124G>T	ENSP00000454971.1:p.Ala42Ser
ENST00000568375.1:n.142G>T
NM_020988.2:c.904G>T	NP_066268.1:p.Ala302Ser
XM_011523003.1:c.778G>T	XP_011521305.1:p.Ala260Ser
XM_011523003.3:c.778G>T	XP_011521305.1:p.Ala260Ser
NM_020988.3:c.904G>T MANE Select	NP_066268.1:p.Ala302Ser