Canonical Allele Identifier: CA721980768

Gene: GNAO1

Linked Data

• dbSNP Id: rs1194046467
• MyVariant Identifiers: chr16:g.56370975_56370998del (hg19) ; chr16:g.56337063_56337086del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56337064_56337087del , CM000678.2:g.56337064_56337087del	GRCh38
NC_000016.9:g.56370976_56370999del , CM000678.1:g.56370976_56370999del	GRCh37
NC_000016.8:g.54928477_54928500del	NCBI36
NG_042800.1:g.150726_150749del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.723+204_723+227del	ENSP00000262494.7:n.723+204_723+227del
ENST00000262493.12:c.723+204_723+227del MANE Select	ENSP00000262493.6:n.723+204_723+227del
ENST00000262494.12:c.723+204_723+227del	ENSP00000262494.7:n.723+204_723+227del
ENST00000562316.6:c.390+204_390+227del	ENSP00000457238.2:n.390+204_390+227del
ENST00000564727.2:c.27+204_27+227del	ENSP00000454971.2:n.27+204_27+227del
ENST00000568375.2:c.115+204_115+227del
ENST00000638185.1:n.938+204_938+227del
ENST00000638210.1:n.1023+204_1023+227del
ENST00000638705.1:c.723+204_723+227del	ENSP00000491223.1:n.723+204_723+227del
ENST00000638836.1:n.633+204_633+227del
ENST00000639055.1:n.1444+204_1444+227del
ENST00000639251.1:n.624+204_624+227del
ENST00000639268.1:c.358+204_358+227del
ENST00000639341.1:c.248+204_248+227del
ENST00000639770.1:c.761+204_761+227del	ENSP00000491999.1:n.761+204_761+227del
ENST00000640390.1:n.653+204_653+227del
ENST00000640469.1:c.87+204_87+227del	ENSP00000491875.1:n.87+204_87+227del
ENST00000640560.1:n.499+204_499+227del
ENST00000640893.1:c.*121+204_*121+227del	ENSP00000492677.1:n.*121+204_*121+227del
ENST00000262493.10:c.723+204_723+227del	ENSP00000262493.6:n.723+204_723+227del
ENST00000262494.11:c.723+204_723+227del	ENSP00000262494.7:n.723+204_723+227del
ENST00000568375.1:n.115+204_115+227del
NM_020988.2:c.723+204_723+227del	NP_066268.1:n.723+204_723+227del
NM_138736.2:c.723+204_723+227del	NP_620073.2:n.723+204_723+227del
XM_011523003.1:c.597+204_597+227del	XP_011521305.1:n.597+204_597+227del
XM_011523003.3:c.597+204_597+227del	XP_011521305.1:n.597+204_597+227del
NM_020988.3:c.723+204_723+227del MANE Select	NP_066268.1:n.723+204_723+227del
NM_138736.3:c.723+204_723+227del	NP_620073.2:n.723+204_723+227del