Canonical Allele Identifier: CA395952129

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56370641A>T (hg19) ; chr16:g.56336729A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336729A>T , CM000678.2:g.56336729A>T	GRCh38
NC_000016.9:g.56370641A>T , CM000678.1:g.56370641A>T	GRCh37
NC_000016.8:g.54928142A>T	NCBI36
NG_042800.1:g.150391A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262494.13:c.594-2A>T	ENSP00000262494.7:n.594-2A>T
ENST00000262493.12:c.594-2A>T MANE Select	ENSP00000262493.6:n.594-2A>T
ENST00000262494.12:c.594-2A>T	ENSP00000262494.7:n.594-2A>T
ENST00000562316.6:c.261-2A>T	ENSP00000457238.2:n.261-2A>T
ENST00000638185.1:n.809-2A>T
ENST00000638210.1:n.894-2A>T
ENST00000638705.1:c.594-2A>T	ENSP00000491223.1:n.594-2A>T
ENST00000638836.1:n.504-2A>T
ENST00000639055.1:n.1315-2A>T
ENST00000639251.1:n.495-2A>T
ENST00000639268.1:c.229-2A>T
ENST00000639341.1:c.119-2A>T
ENST00000639770.1:c.632-2A>T	ENSP00000491999.1:n.632-2A>T
ENST00000640390.1:n.524-2A>T
ENST00000640560.1:n.368A>T
ENST00000640893.1:c.433-2A>T	ENSP00000492677.1:n.433-2A>T
ENST00000262493.10:c.594-2A>T	ENSP00000262493.6:n.594-2A>T
ENST00000262494.11:c.594-2A>T	ENSP00000262494.7:n.594-2A>T
NM_020988.2:c.594-2A>T	NP_066268.1:n.594-2A>T
NM_138736.2:c.594-2A>T	NP_620073.2:n.594-2A>T
XM_011523003.1:c.468-2A>T	XP_011521305.1:n.468-2A>T
XM_011523003.3:c.468-2A>T	XP_011521305.1:n.468-2A>T
NM_020988.3:c.594-2A>T MANE Select	NP_066268.1:n.594-2A>T
NM_138736.3:c.594-2A>T	NP_620073.2:n.594-2A>T