Canonical Allele Identifier: CA2633322170

Gene: GNAO1

Linked Data

• gnomAD v4: 16-56351812-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351815_56351816del , CM000678.2:g.56351815_56351816del	GRCh38
NC_000016.9:g.56385727_56385728del , CM000678.1:g.56385727_56385728del	GRCh37
NC_000016.8:g.54943228_54943229del	NCBI36
NG_042800.1:g.165477_165478del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.877+278_877+279del MANE Select	ENSP00000262493.6:n.877+278_877+279del
ENST00000562316.6:c.544+278_544+279del	ENSP00000457238.2:n.544+278_544+279del
ENST00000564727.2:c.181+278_181+279del	ENSP00000454971.2:n.181+278_181+279del
ENST00000568375.2:c.116-3051_116-3050del
ENST00000638185.1:n.1092+278_1092+279del
ENST00000638210.1:n.1177+278_1177+279del
ENST00000638705.1:c.877+278_877+279del	ENSP00000491223.1:n.877+278_877+279del
ENST00000638836.1:n.787+278_787+279del
ENST00000639055.1:n.1598+278_1598+279del
ENST00000639251.1:n.778+278_778+279del
ENST00000639268.1:c.512+278_512+279del
ENST00000639341.1:c.402+278_402+279del
ENST00000639770.1:c.915+278_915+279del	ENSP00000491999.1:n.915+278_915+279del
ENST00000640390.1:n.807+278_807+279del
ENST00000640469.1:c.241+278_241+279del	ENSP00000491875.1:n.241+278_241+279del
ENST00000640560.1:n.653+278_653+279del
ENST00000640893.1:c.*275+278_*275+279del	ENSP00000492677.1:n.*275+278_*275+279del
ENST00000262493.10:c.877+278_877+279del	ENSP00000262493.6:n.877+278_877+279del
ENST00000564727.1:c.97+278_97+279del	ENSP00000454971.1:n.97+278_97+279del
ENST00000568375.1:n.116-3051_116-3050del
NM_020988.2:c.877+278_877+279del	NP_066268.1:n.877+278_877+279del
XM_011523003.1:c.751+278_751+279del	XP_011521305.1:n.751+278_751+279del
XM_011523003.3:c.751+278_751+279del	XP_011521305.1:n.751+278_751+279del
NM_020988.3:c.877+278_877+279del MANE Select	NP_066268.1:n.877+278_877+279del