Canonical Allele Identifier: CA395952221

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56370684G>A (hg19) ; chr16:g.56336772G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336772G>A , CM000678.2:g.56336772G>A	GRCh38
NC_000016.9:g.56370684G>A , CM000678.1:g.56370684G>A	GRCh37
NC_000016.8:g.54928185G>A	NCBI36
NG_042800.1:g.150434G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.635G>A	ENSP00000262494.7:p.Trp212Ter
ENST00000262493.12:c.635G>A MANE Select	ENSP00000262493.6:p.Trp212Ter
ENST00000262494.12:c.635G>A	ENSP00000262494.7:p.Trp212Ter
ENST00000562316.6:c.302G>A	ENSP00000457238.2:p.Trp101Ter
ENST00000568375.2:c.27G>A
ENST00000638185.1:n.850G>A
ENST00000638210.1:n.935G>A
ENST00000638705.1:c.635G>A	ENSP00000491223.1:p.Trp212Ter
ENST00000638836.1:n.545G>A
ENST00000639055.1:n.1356G>A
ENST00000639251.1:n.536G>A
ENST00000639268.1:c.270G>A
ENST00000639341.1:c.160G>A
ENST00000639770.1:c.673G>A	ENSP00000491999.1:n.673G>A
ENST00000640390.1:n.565G>A
ENST00000640560.1:n.411G>A
ENST00000640893.1:c.*33G>A	ENSP00000492677.1:n.*33G>A
ENST00000262493.10:c.635G>A	ENSP00000262493.6:p.Trp212Ter
ENST00000262494.11:c.635G>A	ENSP00000262494.7:p.Trp212Ter
ENST00000568375.1:n.27G>A
NM_020988.2:c.635G>A	NP_066268.1:p.Trp212Ter
NM_138736.2:c.635G>A	NP_620073.2:p.Trp212Ter
XM_011523003.1:c.509G>A	XP_011521305.1:p.Trp170Ter
XM_011523003.3:c.509G>A	XP_011521305.1:p.Trp170Ter
NM_020988.3:c.635G>A MANE Select	NP_066268.1:p.Trp212Ter
NM_138736.3:c.635G>A	NP_620073.2:p.Trp212Ter