Canonical Allele Identifier: CA2633315103

Gene: GNAO1

Linked Data

• gnomAD v4: 16-56336672-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336676del , CM000678.2:g.56336676del	GRCh38
NC_000016.9:g.56370588del , CM000678.1:g.56370588del	GRCh37
NC_000016.8:g.54928089del	NCBI36
NG_042800.1:g.150338del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.594-55del	ENSP00000262494.7:n.594-55del
ENST00000262493.12:c.594-55del MANE Select	ENSP00000262493.6:n.594-55del
ENST00000262494.12:c.594-55del	ENSP00000262494.7:n.594-55del
ENST00000562316.6:c.261-55del	ENSP00000457238.2:n.261-55del
ENST00000638185.1:n.809-55del
ENST00000638210.1:n.894-55del
ENST00000638705.1:c.594-55del	ENSP00000491223.1:n.594-55del
ENST00000638836.1:n.504-55del
ENST00000639055.1:n.1315-55del
ENST00000639251.1:n.495-55del
ENST00000639268.1:c.229-55del
ENST00000639341.1:c.119-55del
ENST00000639770.1:c.632-55del	ENSP00000491999.1:n.632-55del
ENST00000640390.1:n.524-55del
ENST00000640560.1:n.315del
ENST00000640893.1:c.433-55del	ENSP00000492677.1:n.433-55del
ENST00000262493.10:c.594-55del	ENSP00000262493.6:n.594-55del
ENST00000262494.11:c.594-55del	ENSP00000262494.7:n.594-55del
NM_020988.2:c.594-55del	NP_066268.1:n.594-55del
NM_138736.2:c.594-55del	NP_620073.2:n.594-55del
XM_011523003.1:c.468-55del	XP_011521305.1:n.468-55del
XM_011523003.3:c.468-55del	XP_011521305.1:n.468-55del
NM_020988.3:c.594-55del MANE Select	NP_066268.1:n.594-55del
NM_138736.3:c.594-55del	NP_620073.2:n.594-55del