Canonical Allele Identifier: CA395951824

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56368771T>G (hg19) ; chr16:g.56334859T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56334859T>G , CM000678.2:g.56334859T>G	GRCh38
NC_000016.9:g.56368771T>G , CM000678.1:g.56368771T>G	GRCh37
NC_000016.8:g.54926272T>G	NCBI36
NG_042800.1:g.148521T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.593+2T>G	ENSP00000262494.7:n.593+2T>G
ENST00000262493.12:c.593+2T>G MANE Select	ENSP00000262493.6:n.593+2T>G
ENST00000262494.12:c.593+2T>G	ENSP00000262494.7:n.593+2T>G
ENST00000562316.6:c.260+2T>G	ENSP00000457238.2:n.260+2T>G
ENST00000638185.1:n.808+2T>G
ENST00000638210.1:n.893+2T>G
ENST00000638705.1:c.593+2T>G	ENSP00000491223.1:n.593+2T>G
ENST00000638836.1:n.503+2T>G
ENST00000639055.1:n.1314+2T>G
ENST00000639251.1:n.494+2T>G
ENST00000639268.1:c.229-1872T>G
ENST00000639341.1:c.118+2T>G
ENST00000639770.1:c.631+2T>G	ENSP00000491999.1:n.631+2T>G
ENST00000640390.1:n.523+2T>G
ENST00000640893.1:c.432+2T>G	ENSP00000492677.1:n.432+2T>G
ENST00000262493.10:c.593+2T>G	ENSP00000262493.6:n.593+2T>G
ENST00000262494.11:c.593+2T>G	ENSP00000262494.7:n.593+2T>G
NM_020988.2:c.593+2T>G	NP_066268.1:n.593+2T>G
NM_138736.2:c.593+2T>G	NP_620073.2:n.593+2T>G
XM_011523003.1:c.467+2T>G	XP_011521305.1:n.467+2T>G
XM_011523003.3:c.467+2T>G	XP_011521305.1:n.467+2T>G
NM_020988.3:c.593+2T>G MANE Select	NP_066268.1:n.593+2T>G
NM_138736.3:c.593+2T>G	NP_620073.2:n.593+2T>G