Canonical Allele Identifier: CA395952140

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56370647T>A (hg19) ; chr16:g.56336735T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336735T>A , CM000678.2:g.56336735T>A	GRCh38
NC_000016.9:g.56370647T>A , CM000678.1:g.56370647T>A	GRCh37
NC_000016.8:g.54928148T>A	NCBI36
NG_042800.1:g.150397T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.598T>A	ENSP00000262494.7:p.Phe200Ile
ENST00000262493.12:c.598T>A MANE Select	ENSP00000262493.6:p.Phe200Ile
ENST00000262494.12:c.598T>A	ENSP00000262494.7:p.Phe200Ile
ENST00000562316.6:c.265T>A	ENSP00000457238.2:p.Phe89Ile
ENST00000638185.1:n.813T>A
ENST00000638210.1:n.898T>A
ENST00000638705.1:c.598T>A	ENSP00000491223.1:p.Phe200Ile
ENST00000638836.1:n.508T>A
ENST00000639055.1:n.1319T>A
ENST00000639251.1:n.499T>A
ENST00000639268.1:c.233T>A
ENST00000639341.1:c.123T>A
ENST00000639770.1:c.636T>A	ENSP00000491999.1:n.636T>A
ENST00000640390.1:n.528T>A
ENST00000640560.1:n.374T>A
ENST00000640893.1:c.437T>A	ENSP00000492677.1:p.Val146Asp
ENST00000262493.10:c.598T>A	ENSP00000262493.6:p.Phe200Ile
ENST00000262494.11:c.598T>A	ENSP00000262494.7:p.Phe200Ile
NM_020988.2:c.598T>A	NP_066268.1:p.Phe200Ile
NM_138736.2:c.598T>A	NP_620073.2:p.Phe200Ile
XM_011523003.1:c.472T>A	XP_011521305.1:p.Phe158Ile
XM_011523003.3:c.472T>A	XP_011521305.1:p.Phe158Ile
NM_020988.3:c.598T>A MANE Select	NP_066268.1:p.Phe200Ile
NM_138736.3:c.598T>A	NP_620073.2:p.Phe200Ile