Canonical Allele Identifier: CA395951754

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56368756A>C (hg19) ; chr16:g.56334844A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56334844A>C , CM000678.2:g.56334844A>C	GRCh38
NC_000016.9:g.56368756A>C , CM000678.1:g.56368756A>C	GRCh37
NC_000016.8:g.54926257A>C	NCBI36
NG_042800.1:g.148506A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.580A>C	ENSP00000262494.7:p.Asn194His
ENST00000262493.12:c.580A>C MANE Select	ENSP00000262493.6:p.Asn194His
ENST00000262494.12:c.580A>C	ENSP00000262494.7:p.Asn194His
ENST00000562316.6:c.247A>C	ENSP00000457238.2:p.Asn83His
ENST00000638185.1:n.795A>C
ENST00000638210.1:n.880A>C
ENST00000638705.1:c.580A>C	ENSP00000491223.1:p.Asn194His
ENST00000638836.1:n.490A>C
ENST00000639055.1:n.1301A>C
ENST00000639251.1:n.481A>C
ENST00000639268.1:c.229-1887A>C
ENST00000639341.1:c.105A>C
ENST00000639770.1:c.618A>C	ENSP00000491999.1:n.618A>C
ENST00000640390.1:n.510A>C
ENST00000640893.1:c.419A>C	ENSP00000492677.1:p.Glu140Ala
ENST00000262493.10:c.580A>C	ENSP00000262493.6:p.Asn194His
ENST00000262494.11:c.580A>C	ENSP00000262494.7:p.Asn194His
ENST00000562316.5:c.319A>C	ENSP00000457238.1:p.Asn107His
NM_020988.2:c.580A>C	NP_066268.1:p.Asn194His
NM_138736.2:c.580A>C	NP_620073.2:p.Asn194His
XM_011523003.1:c.454A>C	XP_011521305.1:p.Asn152His
XM_011523003.3:c.454A>C	XP_011521305.1:p.Asn152His
NM_020988.3:c.580A>C MANE Select	NP_066268.1:p.Asn194His
NM_138736.3:c.580A>C	NP_620073.2:p.Asn194His