Canonical Allele Identifier: CA281440081

Gene: GNAO1

Linked Data

• dbSNP Id: rs551790092
• gnomAD v4: 16-56351626-G-A
• MyVariant Identifiers: chr16:g.56385538G>A (hg19) ; chr16:g.56351626G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351626G>A , CM000678.2:g.56351626G>A	GRCh38
NC_000016.9:g.56385538G>A , CM000678.1:g.56385538G>A	GRCh37
NC_000016.8:g.54943039G>A	NCBI36
NG_042800.1:g.165288G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.877+89G>A MANE Select	ENSP00000262493.6:n.877+89G>A
ENST00000562316.6:c.544+89G>A	ENSP00000457238.2:n.544+89G>A
ENST00000564727.2:c.181+89G>A	ENSP00000454971.2:n.181+89G>A
ENST00000568375.2:c.116-3240G>A
ENST00000638185.1:n.1092+89G>A
ENST00000638210.1:n.1177+89G>A
ENST00000638705.1:c.877+89G>A	ENSP00000491223.1:n.877+89G>A
ENST00000638836.1:n.787+89G>A
ENST00000639055.1:n.1598+89G>A
ENST00000639251.1:n.778+89G>A
ENST00000639268.1:c.512+89G>A
ENST00000639341.1:c.402+89G>A
ENST00000639770.1:c.915+89G>A	ENSP00000491999.1:n.915+89G>A
ENST00000640390.1:n.807+89G>A
ENST00000640469.1:c.241+89G>A	ENSP00000491875.1:n.241+89G>A
ENST00000640560.1:n.653+89G>A
ENST00000640893.1:c.*275+89G>A	ENSP00000492677.1:n.*275+89G>A
ENST00000262493.10:c.877+89G>A	ENSP00000262493.6:n.877+89G>A
ENST00000564727.1:c.97+89G>A	ENSP00000454971.1:n.97+89G>A
ENST00000568375.1:n.116-3240G>A
NM_020988.2:c.877+89G>A	NP_066268.1:n.877+89G>A
XM_011523003.1:c.751+89G>A	XP_011521305.1:n.751+89G>A
XM_011523003.3:c.751+89G>A	XP_011521305.1:n.751+89G>A
NM_020988.3:c.877+89G>A MANE Select	NP_066268.1:n.877+89G>A