Canonical Allele Identifier: CA281431414

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56340774C>T , CM000678.2:g.56340774C>T	GRCh38
NC_000016.9:g.56374686C>T , CM000678.1:g.56374686C>T	GRCh37
NC_000016.8:g.54932187C>T	NCBI36
NG_042800.1:g.154436C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020988.3:c.723+3914C>T MANE Select	NP_066268.1:n.723+3914C>T
ENST00000262493.12:c.723+3914C>T MANE Select	ENSP00000262493.6:n.723+3914C>T
NM_020988.2:c.723+3914C>T	NP_066268.1:n.723+3914C>T
NM_138736.2:c.724-60C>T	NP_620073.2:n.724-60C>T
NM_138736.3:c.724-60C>T	NP_620073.2:n.724-60C>T
ENST00000262493.10:c.723+3914C>T	ENSP00000262493.6:n.723+3914C>T
ENST00000262494.11:c.724-60C>T	ENSP00000262494.7:n.724-60C>T
ENST00000262494.12:c.724-60C>T	ENSP00000262494.7:n.724-60C>T
ENST00000262494.13:c.724-60C>T	ENSP00000262494.7:n.724-60C>T
ENST00000562316.6:c.390+3914C>T	ENSP00000457238.2:n.390+3914C>T
ENST00000564727.2:c.27+3914C>T	ENSP00000454971.2:n.27+3914C>T
ENST00000564798.1:n.479C>T
ENST00000564798.2:n.479C>T
ENST00000568375.1:n.115+3914C>T
ENST00000568375.2:c.115+3914C>T
ENST00000638185.1:n.938+3914C>T
ENST00000638210.1:n.1023+3914C>T
ENST00000638705.1:c.723+3914C>T	ENSP00000491223.1:n.723+3914C>T
ENST00000638836.1:n.633+3914C>T
ENST00000639055.1:n.1444+3914C>T
ENST00000639251.1:n.624+3914C>T
ENST00000639268.1:c.358+3914C>T
ENST00000639341.1:c.248+3914C>T
ENST00000639770.1:c.761+3914C>T	ENSP00000491999.1:n.761+3914C>T
ENST00000639787.1:n.69-60C>T
ENST00000640390.1:n.653+3914C>T
ENST00000640469.1:c.87+3914C>T	ENSP00000491875.1:n.87+3914C>T
ENST00000640560.1:n.499+3914C>T
ENST00000640893.1:c.*121+3914C>T	ENSP00000492677.1:n.*121+3914C>T
XM_011523003.1:c.597+3914C>T	XP_011521305.1:n.597+3914C>T
XM_011523003.3:c.597+3914C>T	XP_011521305.1:n.597+3914C>T