Canonical Allele Identifier: CA721980752

Gene: GNAO1

Linked Data

• dbSNP Id: rs1271239568
• MyVariant Identifiers: chr16:g.56370949_56370960del (hg19) ; chr16:g.56337037_56337048del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56337041_56337052del , CM000678.2:g.56337041_56337052del	GRCh38
NC_000016.9:g.56370953_56370964del , CM000678.1:g.56370953_56370964del	GRCh37
NC_000016.8:g.54928454_54928465del	NCBI36
NG_042800.1:g.150703_150714del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.723+181_723+192del	ENSP00000262494.7:n.723+181_723+192del
ENST00000262493.12:c.723+181_723+192del MANE Select	ENSP00000262493.6:n.723+181_723+192del
ENST00000262494.12:c.723+181_723+192del	ENSP00000262494.7:n.723+181_723+192del
ENST00000562316.6:c.390+181_390+192del	ENSP00000457238.2:n.390+181_390+192del
ENST00000564727.2:c.27+181_27+192del	ENSP00000454971.2:n.27+181_27+192del
ENST00000568375.2:c.115+181_115+192del
ENST00000638185.1:n.938+181_938+192del
ENST00000638210.1:n.1023+181_1023+192del
ENST00000638705.1:c.723+181_723+192del	ENSP00000491223.1:n.723+181_723+192del
ENST00000638836.1:n.633+181_633+192del
ENST00000639055.1:n.1444+181_1444+192del
ENST00000639251.1:n.624+181_624+192del
ENST00000639268.1:c.358+181_358+192del
ENST00000639341.1:c.248+181_248+192del
ENST00000639770.1:c.761+181_761+192del	ENSP00000491999.1:n.761+181_761+192del
ENST00000640390.1:n.653+181_653+192del
ENST00000640469.1:c.87+181_87+192del	ENSP00000491875.1:n.87+181_87+192del
ENST00000640560.1:n.499+181_499+192del
ENST00000640893.1:c.*121+181_*121+192del	ENSP00000492677.1:n.*121+181_*121+192del
ENST00000262493.10:c.723+181_723+192del	ENSP00000262493.6:n.723+181_723+192del
ENST00000262494.11:c.723+181_723+192del	ENSP00000262494.7:n.723+181_723+192del
ENST00000568375.1:n.115+181_115+192del
NM_020988.2:c.723+181_723+192del	NP_066268.1:n.723+181_723+192del
NM_138736.2:c.723+181_723+192del	NP_620073.2:n.723+181_723+192del
XM_011523003.1:c.597+181_597+192del	XP_011521305.1:n.597+181_597+192del
XM_011523003.3:c.597+181_597+192del	XP_011521305.1:n.597+181_597+192del
NM_020988.3:c.723+181_723+192del MANE Select	NP_066268.1:n.723+181_723+192del
NM_138736.3:c.723+181_723+192del	NP_620073.2:n.723+181_723+192del