Canonical Allele Identifier: CA395952148

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56370650G>A (hg19) ; chr16:g.56336738G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336738G>A , CM000678.2:g.56336738G>A	GRCh38
NC_000016.9:g.56370650G>A , CM000678.1:g.56370650G>A	GRCh37
NC_000016.8:g.54928151G>A	NCBI36
NG_042800.1:g.150400G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.601G>A	ENSP00000262494.7:p.Asp201Asn
ENST00000262493.12:c.601G>A MANE Select	ENSP00000262493.6:p.Asp201Asn
ENST00000262494.12:c.601G>A	ENSP00000262494.7:p.Asp201Asn
ENST00000562316.6:c.268G>A	ENSP00000457238.2:p.Asp90Asn
ENST00000638185.1:n.816G>A
ENST00000638210.1:n.901G>A
ENST00000638705.1:c.601G>A	ENSP00000491223.1:p.Asp201Asn
ENST00000638836.1:n.511G>A
ENST00000639055.1:n.1322G>A
ENST00000639251.1:n.502G>A
ENST00000639268.1:c.236G>A
ENST00000639341.1:c.126G>A
ENST00000639770.1:c.639G>A	ENSP00000491999.1:n.639G>A
ENST00000640390.1:n.531G>A
ENST00000640560.1:n.377G>A
ENST00000640893.1:c.440G>A	ENSP00000492677.1:p.Ter147=
ENST00000262493.10:c.601G>A	ENSP00000262493.6:p.Asp201Asn
ENST00000262494.11:c.601G>A	ENSP00000262494.7:p.Asp201Asn
NM_020988.2:c.601G>A	NP_066268.1:p.Asp201Asn
NM_138736.2:c.601G>A	NP_620073.2:p.Asp201Asn
XM_011523003.1:c.475G>A	XP_011521305.1:p.Asp159Asn
XM_011523003.3:c.475G>A	XP_011521305.1:p.Asp159Asn
NM_020988.3:c.601G>A MANE Select	NP_066268.1:p.Asp201Asn
NM_138736.3:c.601G>A	NP_620073.2:p.Asp201Asn