Canonical Allele Identifier: CA281426606

Gene: GNAO1

Linked Data

• dbSNP Id: rs907681782
• MyVariant Identifiers: chr16:g.56368559A>T (hg19) ; chr16:g.56334647A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56334647A>T , CM000678.2:g.56334647A>T	GRCh38
NC_000016.9:g.56368559A>T , CM000678.1:g.56368559A>T	GRCh37
NC_000016.8:g.54926060A>T	NCBI36
NG_042800.1:g.148309A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.465-82A>T	ENSP00000262494.7:n.465-82A>T
ENST00000262493.12:c.465-82A>T MANE Select	ENSP00000262493.6:n.465-82A>T
ENST00000262494.12:c.465-82A>T	ENSP00000262494.7:n.465-82A>T
ENST00000562316.6:c.132-82A>T	ENSP00000457238.2:n.132-82A>T
ENST00000638185.1:n.680-82A>T
ENST00000638210.1:n.765-82A>T
ENST00000638705.1:c.465-82A>T	ENSP00000491223.1:n.465-82A>T
ENST00000638836.1:n.375-82A>T
ENST00000639055.1:n.1186-82A>T
ENST00000639251.1:n.366-82A>T
ENST00000639268.1:c.229-2084A>T
ENST00000639770.1:c.503-82A>T	ENSP00000491999.1:n.503-82A>T
ENST00000640390.1:n.395-82A>T
ENST00000640893.1:c.304-82A>T	ENSP00000492677.1:n.304-82A>T
ENST00000262493.10:c.465-82A>T	ENSP00000262493.6:n.465-82A>T
ENST00000262494.11:c.465-82A>T	ENSP00000262494.7:n.465-82A>T
ENST00000562316.5:c.204-82A>T	ENSP00000457238.1:n.204-82A>T
ENST00000563440.1:c.204-82A>T	ENSP00000455774.1:n.204-82A>T
ENST00000565363.5:c.339-82A>T	ENSP00000454728.1:n.339-82A>T
NM_020988.2:c.465-82A>T	NP_066268.1:n.465-82A>T
NM_138736.2:c.465-82A>T	NP_620073.2:n.465-82A>T
XM_011523003.1:c.339-82A>T	XP_011521305.1:n.339-82A>T
XM_011523003.3:c.339-82A>T	XP_011521305.1:n.339-82A>T
NM_020988.3:c.465-82A>T MANE Select	NP_066268.1:n.465-82A>T
NM_138736.3:c.465-82A>T	NP_620073.2:n.465-82A>T