Canonical Allele Identifier: CA395954961

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56388783A>G (hg19) ; chr16:g.56354871A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56354871A>G , CM000678.2:g.56354871A>G	GRCh38
NC_000016.9:g.56388783A>G , CM000678.1:g.56388783A>G	GRCh37
NC_000016.8:g.54946284A>G	NCBI36
NG_042800.1:g.168533A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000262493.12:c.883A>G MANE Select	ENSP00000262493.6:p.Asn295Asp
ENST00000562316.6:c.545-1232A>G	ENSP00000457238.2:n.545-1232A>G
ENST00000564727.2:c.187A>G	ENSP00000454971.2:p.Asn63Asp
ENST00000568375.2:c.121A>G
ENST00000638185.1:n.1098A>G
ENST00000638210.1:n.1183A>G
ENST00000638705.1:c.883A>G	ENSP00000491223.1:p.Asn295Asp
ENST00000638836.1:n.793A>G
ENST00000639055.1:n.1604A>G
ENST00000639251.1:n.784A>G
ENST00000639268.1:c.518A>G
ENST00000639341.1:c.408A>G
ENST00000639770.1:c.921A>G	ENSP00000491999.1:n.921A>G
ENST00000640390.1:n.813A>G
ENST00000640469.1:c.247A>G	ENSP00000491875.1:p.Asn83Asp
ENST00000640560.1:n.659A>G
ENST00000640893.1:c.*281A>G	ENSP00000492677.1:n.*281A>G
ENST00000262493.10:c.883A>G	ENSP00000262493.6:p.Asn295Asp
ENST00000564727.1:c.103A>G	ENSP00000454971.1:p.Asn35Asp
ENST00000568375.1:n.121A>G
NM_020988.2:c.883A>G	NP_066268.1:p.Asn295Asp
XM_011523003.1:c.757A>G	XP_011521305.1:p.Asn253Asp
XM_011523003.3:c.757A>G	XP_011521305.1:p.Asn253Asp
NM_020988.3:c.883A>G MANE Select	NP_066268.1:p.Asn295Asp