Canonical Allele Identifier: CA2224108953

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351962_56351979delinsGGGCCTGGACTGCCTCTT , CM000678.2:g.56351962_56351979delinsGGGCCTGGACTGCCTCTT	GRCh38
NC_000016.9:g.56385874_56385891delinsGGGCCTGGACTGCCTCTT , CM000678.1:g.56385874_56385891delinsGGGCCTGGACTGCCTCTT	GRCh37
NC_000016.8:g.54943375_54943392delinsGGGCCTGGACTGCCTCTT	NCBI36
NG_042800.1:g.165624_165641delinsGGGCCTGGACTGCCTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.877+425_877+442delinsGGGCCTGGACTGCCTCTT MANE Select	ENSP00000262493.6:n.877+425_877+442delinsGGGCCTGGACTGCCTCTT
ENST00000562316.6:c.544+425_544+442delinsGGGCCTGGACTGCCTCTT	ENSP00000457238.2:n.544+425_544+442delinsGGGCCTGGACTGCCTCTT
ENST00000564727.2:c.181+425_181+442delinsGGGCCTGGACTGCCTCTT	ENSP00000454971.2:n.181+425_181+442delinsGGGCCTGGACTGCCTCTT
ENST00000568375.2:c.116-2904_116-2887delinsGGGCCTGGACTGCCTCTT
ENST00000638185.1:n.1092+425_1092+442delinsGGGCCTGGACTGCCTCTT
ENST00000638210.1:n.1177+425_1177+442delinsGGGCCTGGACTGCCTCTT
ENST00000638705.1:c.877+425_877+442delinsGGGCCTGGACTGCCTCTT	ENSP00000491223.1:n.877+425_877+442delinsGGGCCTGGACTGCCTCTT
ENST00000638836.1:n.787+425_787+442delinsGGGCCTGGACTGCCTCTT
ENST00000639055.1:n.1598+425_1598+442delinsGGGCCTGGACTGCCTCTT
ENST00000639251.1:n.778+425_778+442delinsGGGCCTGGACTGCCTCTT
ENST00000639268.1:c.512+425_512+442delinsGGGCCTGGACTGCCTCTT
ENST00000639341.1:c.402+425_402+442delinsGGGCCTGGACTGCCTCTT
ENST00000639770.1:c.915+425_915+442delinsGGGCCTGGACTGCCTCTT	ENSP00000491999.1:n.915+425_915+442delinsGGGCCTGGACTGCCTCTT
ENST00000640390.1:n.807+425_807+442delinsGGGCCTGGACTGCCTCTT
ENST00000640469.1:c.241+425_241+442delinsGGGCCTGGACTGCCTCTT	ENSP00000491875.1:n.241+425_241+442delinsGGGCCTGGACTGCCTCTT
ENST00000640560.1:n.653+425_653+442delinsGGGCCTGGACTGCCTCTT
ENST00000640893.1:c.*275+425_*275+442delinsGGGCCTGGACTGCCTCTT	ENSP00000492677.1:n.*275+425_*275+442delinsGGGCCTGGACTGCCTCTT...
ENST00000262493.10:c.877+425_877+442delinsGGGCCTGGACTGCCTCTT	ENSP00000262493.6:n.877+425_877+442delinsGGGCCTGGACTGCCTCTT
ENST00000564727.1:c.97+425_97+442delinsGGGCCTGGACTGCCTCTT	ENSP00000454971.1:n.97+425_97+442delinsGGGCCTGGACTGCCTCTT
ENST00000568375.1:n.116-2904_116-2887delinsGGGCCTGGACTGCCTCTT
NM_020988.2:c.877+425_877+442delinsGGGCCTGGACTGCCTCTT	NP_066268.1:n.877+425_877+442delinsGGGCCTGGACTGCCTCTT
XM_011523003.1:c.751+425_751+442delinsGGGCCTGGACTGCCTCTT	XP_011521305.1:n.751+425_751+442delinsGGGCCTGGACTGCCTCTT
XM_011523003.3:c.751+425_751+442delinsGGGCCTGGACTGCCTCTT	XP_011521305.1:n.751+425_751+442delinsGGGCCTGGACTGCCTCTT
NM_020988.3:c.877+425_877+442delinsGGGCCTGGACTGCCTCTT MANE Select	NP_066268.1:n.877+425_877+442delinsGGGCCTGGACTGCCTCTT