Canonical Allele Identifier: CA281439766

Gene: GNAO1

Linked Data

• dbSNP Id: rs568597817
• gnomAD v2: 16-56385105-G-A
• gnomAD v3: 16-56351193-G-A
• gnomAD v4: 16-56351193-G-A
• MyVariant Identifiers: chr16:g.56385105G>A (hg19) ; chr16:g.56351193G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351193G>A , CM000678.2:g.56351193G>A	GRCh38
NC_000016.9:g.56385105G>A , CM000678.1:g.56385105G>A	GRCh37
NC_000016.8:g.54942606G>A	NCBI36
NG_042800.1:g.164855G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.724-191G>A MANE Select	ENSP00000262493.6:n.724-191G>A
ENST00000562316.6:c.391-191G>A	ENSP00000457238.2:n.391-191G>A
ENST00000564727.2:c.28-191G>A	ENSP00000454971.2:n.28-191G>A
ENST00000568375.2:c.116-3673G>A
ENST00000638185.1:n.939-191G>A
ENST00000638210.1:n.1024-191G>A
ENST00000638705.1:c.724-191G>A	ENSP00000491223.1:n.724-191G>A
ENST00000638836.1:n.634-191G>A
ENST00000639055.1:n.1445-191G>A
ENST00000639251.1:n.625-191G>A
ENST00000639268.1:c.359-191G>A
ENST00000639341.1:c.249-191G>A
ENST00000639770.1:c.762-191G>A	ENSP00000491999.1:n.762-191G>A
ENST00000640390.1:n.654-191G>A
ENST00000640469.1:c.88-191G>A	ENSP00000491875.1:n.88-191G>A
ENST00000640560.1:n.500-191G>A
ENST00000640893.1:c.*122-191G>A	ENSP00000492677.1:n.*122-191G>A
ENST00000262493.10:c.724-191G>A	ENSP00000262493.6:n.724-191G>A
ENST00000568375.1:n.116-3673G>A
NM_020988.2:c.724-191G>A	NP_066268.1:n.724-191G>A
XM_011523003.1:c.598-191G>A	XP_011521305.1:n.598-191G>A
XM_011523003.3:c.598-191G>A	XP_011521305.1:n.598-191G>A
NM_020988.3:c.724-191G>A MANE Select	NP_066268.1:n.724-191G>A