Canonical Allele Identifier: CA281426490

Gene: GNAO1

Linked Data

• dbSNP Id: rs770468176
• gnomAD v3: 16-56334434-AAAC-A
• gnomAD v4: 16-56334434-AAAC-A
• MyVariant Identifiers: chr16:g.56368347_56368349del (hg19) ; chr16:g.56334435_56334437del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56334436_56334438del , CM000678.2:g.56334436_56334438del	GRCh38
NC_000016.9:g.56368348_56368350del , CM000678.1:g.56368348_56368350del	GRCh37
NC_000016.8:g.54925849_54925851del	NCBI36
NG_042800.1:g.148098_148100del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.465-293_465-291del	ENSP00000262494.7:n.465-293_465-291del
ENST00000262493.12:c.465-293_465-291del MANE Select	ENSP00000262493.6:n.465-293_465-291del
ENST00000262494.12:c.465-293_465-291del	ENSP00000262494.7:n.465-293_465-291del
ENST00000562316.6:c.132-293_132-291del	ENSP00000457238.2:n.132-293_132-291del
ENST00000638185.1:n.680-293_680-291del
ENST00000638210.1:n.765-293_765-291del
ENST00000638705.1:c.465-293_465-291del	ENSP00000491223.1:n.465-293_465-291del
ENST00000638836.1:n.375-293_375-291del
ENST00000639055.1:n.1186-293_1186-291del
ENST00000639251.1:n.366-293_366-291del
ENST00000639268.1:c.229-2295_229-2293del
ENST00000639770.1:c.503-293_503-291del	ENSP00000491999.1:n.503-293_503-291del
ENST00000640390.1:n.395-293_395-291del
ENST00000640893.1:c.304-293_304-291del	ENSP00000492677.1:n.304-293_304-291del
ENST00000262493.10:c.465-293_465-291del	ENSP00000262493.6:n.465-293_465-291del
ENST00000262494.11:c.465-293_465-291del	ENSP00000262494.7:n.465-293_465-291del
ENST00000562316.5:c.204-293_204-291del	ENSP00000457238.1:n.204-293_204-291del
ENST00000563440.1:c.204-293_204-291del	ENSP00000455774.1:n.204-293_204-291del
ENST00000565363.5:c.339-293_339-291del	ENSP00000454728.1:n.339-293_339-291del
NM_020988.2:c.465-293_465-291del	NP_066268.1:n.465-293_465-291del
NM_138736.2:c.465-293_465-291del	NP_620073.2:n.465-293_465-291del
XM_011523003.1:c.339-293_339-291del	XP_011521305.1:n.339-293_339-291del
XM_011523003.3:c.339-293_339-291del	XP_011521305.1:n.339-293_339-291del
NM_020988.3:c.465-293_465-291del MANE Select	NP_066268.1:n.465-293_465-291del
NM_138736.3:c.465-293_465-291del	NP_620073.2:n.465-293_465-291del