Canonical Allele Identifier: CA2807145120

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351889_56351890del , CM000678.2:g.56351889_56351890del	GRCh38
NC_000016.9:g.56385801_56385802del , CM000678.1:g.56385801_56385802del	GRCh37
NC_000016.8:g.54943302_54943303del	NCBI36
NG_042800.1:g.165551_165552del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.877+352_877+353del MANE Select	ENSP00000262493.6:n.877+352_877+353del
ENST00000562316.6:c.544+352_544+353del	ENSP00000457238.2:n.544+352_544+353del
ENST00000564727.2:c.181+352_181+353del	ENSP00000454971.2:n.181+352_181+353del
ENST00000568375.2:c.116-2977_116-2976del
ENST00000638185.1:n.1092+352_1092+353del
ENST00000638210.1:n.1177+352_1177+353del
ENST00000638705.1:c.877+352_877+353del	ENSP00000491223.1:n.877+352_877+353del
ENST00000638836.1:n.787+352_787+353del
ENST00000639055.1:n.1598+352_1598+353del
ENST00000639251.1:n.778+352_778+353del
ENST00000639268.1:c.512+352_512+353del
ENST00000639341.1:c.402+352_402+353del
ENST00000639770.1:c.915+352_915+353del	ENSP00000491999.1:n.915+352_915+353del
ENST00000640390.1:n.807+352_807+353del
ENST00000640469.1:c.241+352_241+353del	ENSP00000491875.1:n.241+352_241+353del
ENST00000640560.1:n.653+352_653+353del
ENST00000640893.1:c.*275+352_*275+353del	ENSP00000492677.1:n.*275+352_*275+353del
ENST00000262493.10:c.877+352_877+353del	ENSP00000262493.6:n.877+352_877+353del
ENST00000564727.1:c.97+352_97+353del	ENSP00000454971.1:n.97+352_97+353del
ENST00000568375.1:n.116-2977_116-2976del
NM_020988.2:c.877+352_877+353del	NP_066268.1:n.877+352_877+353del
XM_011523003.1:c.751+352_751+353del	XP_011521305.1:n.751+352_751+353del
XM_011523003.3:c.751+352_751+353del	XP_011521305.1:n.751+352_751+353del
NM_020988.3:c.877+352_877+353del MANE Select	NP_066268.1:n.877+352_877+353del