Canonical Allele Identifier: CA2633322120

Gene: GNAO1

Linked Data

• gnomAD v4: 16-56351768-ACCAAGTGACTCAGGAGTGGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351769_56351788del , CM000678.2:g.56351769_56351788del	GRCh38
NC_000016.9:g.56385681_56385700del , CM000678.1:g.56385681_56385700del	GRCh37
NC_000016.8:g.54943182_54943201del	NCBI36
NG_042800.1:g.165431_165450del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.877+232_877+251del MANE Select	ENSP00000262493.6:n.877+232_877+251del
ENST00000562316.6:c.544+232_544+251del	ENSP00000457238.2:n.544+232_544+251del
ENST00000564727.2:c.181+232_181+251del	ENSP00000454971.2:n.181+232_181+251del
ENST00000568375.2:c.116-3097_116-3078del
ENST00000638185.1:n.1092+232_1092+251del
ENST00000638210.1:n.1177+232_1177+251del
ENST00000638705.1:c.877+232_877+251del	ENSP00000491223.1:n.877+232_877+251del
ENST00000638836.1:n.787+232_787+251del
ENST00000639055.1:n.1598+232_1598+251del
ENST00000639251.1:n.778+232_778+251del
ENST00000639268.1:c.512+232_512+251del
ENST00000639341.1:c.402+232_402+251del
ENST00000639770.1:c.915+232_915+251del	ENSP00000491999.1:n.915+232_915+251del
ENST00000640390.1:n.807+232_807+251del
ENST00000640469.1:c.241+232_241+251del	ENSP00000491875.1:n.241+232_241+251del
ENST00000640560.1:n.653+232_653+251del
ENST00000640893.1:c.*275+232_*275+251del	ENSP00000492677.1:n.*275+232_*275+251del
ENST00000262493.10:c.877+232_877+251del	ENSP00000262493.6:n.877+232_877+251del
ENST00000564727.1:c.97+232_97+251del	ENSP00000454971.1:n.97+232_97+251del
ENST00000568375.1:n.116-3097_116-3078del
NM_020988.2:c.877+232_877+251del	NP_066268.1:n.877+232_877+251del
XM_011523003.1:c.751+232_751+251del	XP_011521305.1:n.751+232_751+251del
XM_011523003.3:c.751+232_751+251del	XP_011521305.1:n.751+232_751+251del
NM_020988.3:c.877+232_877+251del MANE Select	NP_066268.1:n.877+232_877+251del