Canonical Allele Identifier: CA395954963

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56388784A>C (hg19) ; chr16:g.56354872A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56354872A>C , CM000678.2:g.56354872A>C	GRCh38
NC_000016.9:g.56388784A>C , CM000678.1:g.56388784A>C	GRCh37
NC_000016.8:g.54946285A>C	NCBI36
NG_042800.1:g.168534A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000262493.12:c.884A>C MANE Select	ENSP00000262493.6:p.Asn295Thr
ENST00000562316.6:c.545-1231A>C	ENSP00000457238.2:n.545-1231A>C
ENST00000564727.2:c.188A>C	ENSP00000454971.2:p.Asn63Thr
ENST00000568375.2:c.122A>C
ENST00000638185.1:n.1099A>C
ENST00000638210.1:n.1184A>C
ENST00000638705.1:c.884A>C	ENSP00000491223.1:p.Asn295Thr
ENST00000638836.1:n.794A>C
ENST00000639055.1:n.1605A>C
ENST00000639251.1:n.785A>C
ENST00000639268.1:c.519A>C
ENST00000639341.1:c.409A>C
ENST00000639770.1:c.922A>C	ENSP00000491999.1:n.922A>C
ENST00000640390.1:n.814A>C
ENST00000640469.1:c.248A>C	ENSP00000491875.1:p.Asn83Thr
ENST00000640560.1:n.660A>C
ENST00000640893.1:c.*282A>C	ENSP00000492677.1:n.*282A>C
ENST00000262493.10:c.884A>C	ENSP00000262493.6:p.Asn295Thr
ENST00000564727.1:c.104A>C	ENSP00000454971.1:p.Asn35Thr
ENST00000568375.1:n.122A>C
NM_020988.2:c.884A>C	NP_066268.1:p.Asn295Thr
XM_011523003.1:c.758A>C	XP_011521305.1:p.Asn253Thr
XM_011523003.3:c.758A>C	XP_011521305.1:p.Asn253Thr
NM_020988.3:c.884A>C MANE Select	NP_066268.1:p.Asn295Thr