Canonical Allele Identifier: CA495573652

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56370739C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336827C>T , CM000678.2:g.56336827C>T	GRCh38
NC_000016.9:g.56370739C>T , CM000678.1:g.56370739C>T	GRCh37
NC_000016.8:g.54928240C>T	NCBI36
NG_042800.1:g.150489C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.690C>T	ENSP00000262494.7:p.Gly230=
ENST00000262493.12:c.690C>T MANE Select	ENSP00000262493.6:p.Gly230=
ENST00000262494.12:c.690C>T	ENSP00000262494.7:p.Gly230=
ENST00000562316.6:c.357C>T	ENSP00000457238.2:p.Gly119=
ENST00000568375.2:c.82C>T
ENST00000638185.1:n.905C>T
ENST00000638210.1:n.990C>T
ENST00000638705.1:c.690C>T	ENSP00000491223.1:p.Gly230=
ENST00000638836.1:n.600C>T
ENST00000639055.1:n.1411C>T
ENST00000639251.1:n.591C>T
ENST00000639268.1:c.325C>T
ENST00000639341.1:c.215C>T
ENST00000639770.1:c.728C>T	ENSP00000491999.1:n.728C>T
ENST00000640390.1:n.620C>T
ENST00000640469.1:c.54C>T	ENSP00000491875.1:p.Gly18=
ENST00000640560.1:n.466C>T
ENST00000640893.1:c.*88C>T	ENSP00000492677.1:n.*88C>T
ENST00000262493.10:c.690C>T	ENSP00000262493.6:p.Gly230=
ENST00000262494.11:c.690C>T	ENSP00000262494.7:p.Gly230=
ENST00000568375.1:n.82C>T
NM_020988.2:c.690C>T	NP_066268.1:p.Gly230=
NM_138736.2:c.690C>T	NP_620073.2:p.Gly230=
XM_011523003.1:c.564C>T	XP_011521305.1:p.Gly188=
XM_011523003.3:c.564C>T	XP_011521305.1:p.Gly188=
NM_020988.3:c.690C>T MANE Select	NP_066268.1:p.Gly230=
NM_138736.3:c.690C>T	NP_620073.2:p.Gly230=