Canonical Allele Identifier: CA2575998602

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351613_56351615del , CM000678.2:g.56351613_56351615del	GRCh38
NC_000016.9:g.56385525_56385527del , CM000678.1:g.56385525_56385527del	GRCh37
NC_000016.8:g.54943026_54943028del	NCBI36
NG_042800.1:g.165275_165277del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.877+76_877+78del MANE Select	ENSP00000262493.6:n.877+76_877+78del
ENST00000562316.6:c.544+76_544+78del	ENSP00000457238.2:n.544+76_544+78del
ENST00000564727.2:c.181+76_181+78del	ENSP00000454971.2:n.181+76_181+78del
ENST00000568375.2:c.116-3253_116-3251del
ENST00000638185.1:n.1092+76_1092+78del
ENST00000638210.1:n.1177+76_1177+78del
ENST00000638705.1:c.877+76_877+78del	ENSP00000491223.1:n.877+76_877+78del
ENST00000638836.1:n.787+76_787+78del
ENST00000639055.1:n.1598+76_1598+78del
ENST00000639251.1:n.778+76_778+78del
ENST00000639268.1:c.512+76_512+78del
ENST00000639341.1:c.402+76_402+78del
ENST00000639770.1:c.915+76_915+78del	ENSP00000491999.1:n.915+76_915+78del
ENST00000640390.1:n.807+76_807+78del
ENST00000640469.1:c.241+76_241+78del	ENSP00000491875.1:n.241+76_241+78del
ENST00000640560.1:n.653+76_653+78del
ENST00000640893.1:c.*275+76_*275+78del	ENSP00000492677.1:n.*275+76_*275+78del
ENST00000262493.10:c.877+76_877+78del	ENSP00000262493.6:n.877+76_877+78del
ENST00000564727.1:c.97+76_97+78del	ENSP00000454971.1:n.97+76_97+78del
ENST00000568375.1:n.116-3253_116-3251del
NM_020988.2:c.877+76_877+78del	NP_066268.1:n.877+76_877+78del
XM_011523003.1:c.751+76_751+78del	XP_011521305.1:n.751+76_751+78del
XM_011523003.3:c.751+76_751+78del	XP_011521305.1:n.751+76_751+78del
NM_020988.3:c.877+76_877+78del MANE Select	NP_066268.1:n.877+76_877+78del