Canonical Allele Identifier: CA721991888

Gene: GNAO1

Linked Data

• dbSNP Id: rs1358561408
• MyVariant Identifiers: chr16:g.56385096_56385103del (hg19) ; chr16:g.56351184_56351191del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351186_56351193del , CM000678.2:g.56351186_56351193del	GRCh38
NC_000016.9:g.56385098_56385105del , CM000678.1:g.56385098_56385105del	GRCh37
NC_000016.8:g.54942599_54942606del	NCBI36
NG_042800.1:g.164848_164855del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.724-198_724-191del MANE Select	ENSP00000262493.6:n.724-198_724-191del
ENST00000562316.6:c.391-198_391-191del	ENSP00000457238.2:n.391-198_391-191del
ENST00000564727.2:c.28-198_28-191del	ENSP00000454971.2:n.28-198_28-191del
ENST00000568375.2:c.116-3680_116-3673del
ENST00000638185.1:n.939-198_939-191del
ENST00000638210.1:n.1024-198_1024-191del
ENST00000638705.1:c.724-198_724-191del	ENSP00000491223.1:n.724-198_724-191del
ENST00000638836.1:n.634-198_634-191del
ENST00000639055.1:n.1445-198_1445-191del
ENST00000639251.1:n.625-198_625-191del
ENST00000639268.1:c.359-198_359-191del
ENST00000639341.1:c.249-198_249-191del
ENST00000639770.1:c.762-198_762-191del	ENSP00000491999.1:n.762-198_762-191del
ENST00000640390.1:n.654-198_654-191del
ENST00000640469.1:c.88-198_88-191del	ENSP00000491875.1:n.88-198_88-191del
ENST00000640560.1:n.500-198_500-191del
ENST00000640893.1:c.*122-198_*122-191del	ENSP00000492677.1:n.*122-198_*122-191del
ENST00000262493.10:c.724-198_724-191del	ENSP00000262493.6:n.724-198_724-191del
ENST00000568375.1:n.116-3680_116-3673del
NM_020988.2:c.724-198_724-191del	NP_066268.1:n.724-198_724-191del
XM_011523003.1:c.598-198_598-191del	XP_011521305.1:n.598-198_598-191del
XM_011523003.3:c.598-198_598-191del	XP_011521305.1:n.598-198_598-191del
NM_020988.3:c.724-198_724-191del MANE Select	NP_066268.1:n.724-198_724-191del