Canonical Allele Identifier: CA281426518

Gene: GNAO1

Linked Data

• dbSNP Id: rs373068530
• MyVariant Identifiers: chr16:g.56368366T>C (hg19) ; chr16:g.56334454T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56334454T>C , CM000678.2:g.56334454T>C	GRCh38
NC_000016.9:g.56368366T>C , CM000678.1:g.56368366T>C	GRCh37
NC_000016.8:g.54925867T>C	NCBI36
NG_042800.1:g.148116T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.465-275T>C	ENSP00000262494.7:n.465-275T>C
ENST00000262493.12:c.465-275T>C MANE Select	ENSP00000262493.6:n.465-275T>C
ENST00000262494.12:c.465-275T>C	ENSP00000262494.7:n.465-275T>C
ENST00000562316.6:c.132-275T>C	ENSP00000457238.2:n.132-275T>C
ENST00000638185.1:n.680-275T>C
ENST00000638210.1:n.765-275T>C
ENST00000638705.1:c.465-275T>C	ENSP00000491223.1:n.465-275T>C
ENST00000638836.1:n.375-275T>C
ENST00000639055.1:n.1186-275T>C
ENST00000639251.1:n.366-275T>C
ENST00000639268.1:c.229-2277T>C
ENST00000639770.1:c.503-275T>C	ENSP00000491999.1:n.503-275T>C
ENST00000640390.1:n.395-275T>C
ENST00000640893.1:c.304-275T>C	ENSP00000492677.1:n.304-275T>C
ENST00000262493.10:c.465-275T>C	ENSP00000262493.6:n.465-275T>C
ENST00000262494.11:c.465-275T>C	ENSP00000262494.7:n.465-275T>C
ENST00000562316.5:c.204-275T>C	ENSP00000457238.1:n.204-275T>C
ENST00000563440.1:c.204-275T>C	ENSP00000455774.1:n.204-275T>C
ENST00000565363.5:c.339-275T>C	ENSP00000454728.1:n.339-275T>C
NM_020988.2:c.465-275T>C	NP_066268.1:n.465-275T>C
NM_138736.2:c.465-275T>C	NP_620073.2:n.465-275T>C
XM_011523003.1:c.339-275T>C	XP_011521305.1:n.339-275T>C
XM_011523003.3:c.339-275T>C	XP_011521305.1:n.339-275T>C
NM_020988.3:c.465-275T>C MANE Select	NP_066268.1:n.465-275T>C
NM_138736.3:c.465-275T>C	NP_620073.2:n.465-275T>C