Canonical Allele Identifier: CA622304362

Gene: GNAO1

Linked Data

• dbSNP Id: rs1244828662
• gnomAD v2: 16-56368612-C-T
• gnomAD v4: 16-56334700-C-T
• MyVariant Identifiers: chr16:g.56368612C>T (hg19) ; chr16:g.56334700C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56334700C>T , CM000678.2:g.56334700C>T	GRCh38
NC_000016.9:g.56368612C>T , CM000678.1:g.56368612C>T	GRCh37
NC_000016.8:g.54926113C>T	NCBI36
NG_042800.1:g.148362C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262494.13:c.465-29C>T	ENSP00000262494.7:n.465-29C>T
ENST00000262493.12:c.465-29C>T MANE Select	ENSP00000262493.6:n.465-29C>T
ENST00000262494.12:c.465-29C>T	ENSP00000262494.7:n.465-29C>T
ENST00000562316.6:c.132-29C>T	ENSP00000457238.2:n.132-29C>T
ENST00000638185.1:n.680-29C>T
ENST00000638210.1:n.765-29C>T
ENST00000638705.1:c.465-29C>T	ENSP00000491223.1:n.465-29C>T
ENST00000638836.1:n.375-29C>T
ENST00000639055.1:n.1186-29C>T
ENST00000639251.1:n.366-29C>T
ENST00000639268.1:c.229-2031C>T
ENST00000639770.1:c.503-29C>T	ENSP00000491999.1:n.503-29C>T
ENST00000640390.1:n.395-29C>T
ENST00000640893.1:c.304-29C>T	ENSP00000492677.1:n.304-29C>T
ENST00000262493.10:c.465-29C>T	ENSP00000262493.6:n.465-29C>T
ENST00000262494.11:c.465-29C>T	ENSP00000262494.7:n.465-29C>T
ENST00000562316.5:c.204-29C>T	ENSP00000457238.1:n.204-29C>T
ENST00000563440.1:c.204-29C>T	ENSP00000455774.1:n.204-29C>T
ENST00000565363.5:c.339-29C>T	ENSP00000454728.1:n.339-29C>T
NM_020988.2:c.465-29C>T	NP_066268.1:n.465-29C>T
NM_138736.2:c.465-29C>T	NP_620073.2:n.465-29C>T
XM_011523003.1:c.339-29C>T	XP_011521305.1:n.339-29C>T
XM_011523003.3:c.339-29C>T	XP_011521305.1:n.339-29C>T
NM_020988.3:c.465-29C>T MANE Select	NP_066268.1:n.465-29C>T
NM_138736.3:c.465-29C>T	NP_620073.2:n.465-29C>T