Canonical Allele Identifier: CA395952404

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56370762A>C (hg19) ; chr16:g.56336850A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336850A>C , CM000678.2:g.56336850A>C	GRCh38
NC_000016.9:g.56370762A>C , CM000678.1:g.56370762A>C	GRCh37
NC_000016.8:g.54928263A>C	NCBI36
NG_042800.1:g.150512A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.713A>C	ENSP00000262494.7:p.Asp238Ala
ENST00000262493.12:c.713A>C MANE Select	ENSP00000262493.6:p.Asp238Ala
ENST00000262494.12:c.713A>C	ENSP00000262494.7:p.Asp238Ala
ENST00000562316.6:c.380A>C	ENSP00000457238.2:p.Asp127Ala
ENST00000564727.2:c.17A>C	ENSP00000454971.2:p.Asp6Ala
ENST00000568375.2:c.105A>C
ENST00000638185.1:n.928A>C
ENST00000638210.1:n.1013A>C
ENST00000638705.1:c.713A>C	ENSP00000491223.1:p.Asp238Ala
ENST00000638836.1:n.623A>C
ENST00000639055.1:n.1434A>C
ENST00000639251.1:n.614A>C
ENST00000639268.1:c.348A>C
ENST00000639341.1:c.238A>C
ENST00000639770.1:c.751A>C	ENSP00000491999.1:n.751A>C
ENST00000640390.1:n.643A>C
ENST00000640469.1:c.77A>C	ENSP00000491875.1:p.Asp26Ala
ENST00000640560.1:n.489A>C
ENST00000640893.1:c.*111A>C	ENSP00000492677.1:n.*111A>C
ENST00000262493.10:c.713A>C	ENSP00000262493.6:p.Asp238Ala
ENST00000262494.11:c.713A>C	ENSP00000262494.7:p.Asp238Ala
ENST00000568375.1:n.105A>C
NM_020988.2:c.713A>C	NP_066268.1:p.Asp238Ala
NM_138736.2:c.713A>C	NP_620073.2:p.Asp238Ala
XM_011523003.1:c.587A>C	XP_011521305.1:p.Asp196Ala
XM_011523003.3:c.587A>C	XP_011521305.1:p.Asp196Ala
NM_020988.3:c.713A>C MANE Select	NP_066268.1:p.Asp238Ala
NM_138736.3:c.713A>C	NP_620073.2:p.Asp238Ala