Canonical Allele Identifier: CA2575998597

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351579_56351580insC , CM000678.2:g.56351579_56351580insC	GRCh38
NC_000016.9:g.56385491_56385492insC , CM000678.1:g.56385491_56385492insC	GRCh37
NC_000016.8:g.54942992_54942993insC	NCBI36
NG_042800.1:g.165241_165242insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.877+42_877+43insC MANE Select	ENSP00000262493.6:n.877+42_877+43insC
ENST00000562316.6:c.544+42_544+43insC	ENSP00000457238.2:n.544+42_544+43insC
ENST00000564727.2:c.181+42_181+43insC	ENSP00000454971.2:n.181+42_181+43insC
ENST00000568375.2:c.116-3287_116-3286insC
ENST00000638185.1:n.1092+42_1092+43insC
ENST00000638210.1:n.1177+42_1177+43insC
ENST00000638705.1:c.877+42_877+43insC	ENSP00000491223.1:n.877+42_877+43insC
ENST00000638836.1:n.787+42_787+43insC
ENST00000639055.1:n.1598+42_1598+43insC
ENST00000639251.1:n.778+42_778+43insC
ENST00000639268.1:c.512+42_512+43insC
ENST00000639341.1:c.402+42_402+43insC
ENST00000639770.1:c.915+42_915+43insC	ENSP00000491999.1:n.915+42_915+43insC
ENST00000640390.1:n.807+42_807+43insC
ENST00000640469.1:c.241+42_241+43insC	ENSP00000491875.1:n.241+42_241+43insC
ENST00000640560.1:n.653+42_653+43insC
ENST00000640893.1:c.*275+42_*275+43insC	ENSP00000492677.1:n.*275+42_*275+43insC
ENST00000262493.10:c.877+42_877+43insC	ENSP00000262493.6:n.877+42_877+43insC
ENST00000564727.1:c.97+42_97+43insC	ENSP00000454971.1:n.97+42_97+43insC
ENST00000568375.1:n.116-3287_116-3286insC
NM_020988.2:c.877+42_877+43insC	NP_066268.1:n.877+42_877+43insC
XM_011523003.1:c.751+42_751+43insC	XP_011521305.1:n.751+42_751+43insC
XM_011523003.3:c.751+42_751+43insC	XP_011521305.1:n.751+42_751+43insC
NM_020988.3:c.877+42_877+43insC MANE Select	NP_066268.1:n.877+42_877+43insC