Canonical Allele Identifier: CA395954602

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56385307C>G (hg19) ; chr16:g.56351395C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351395C>G , CM000678.2:g.56351395C>G	GRCh38
NC_000016.9:g.56385307C>G , CM000678.1:g.56385307C>G	GRCh37
NC_000016.8:g.54942808C>G	NCBI36
NG_042800.1:g.165057C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.735C>G MANE Select	ENSP00000262493.6:p.His245Gln
ENST00000562316.6:c.402C>G	ENSP00000457238.2:p.His134Gln
ENST00000564727.2:c.39C>G	ENSP00000454971.2:p.His13Gln
ENST00000568375.2:c.116-3471C>G
ENST00000638185.1:n.950C>G
ENST00000638210.1:n.1035C>G
ENST00000638705.1:c.735C>G	ENSP00000491223.1:p.His245Gln
ENST00000638836.1:n.645C>G
ENST00000639055.1:n.1456C>G
ENST00000639251.1:n.636C>G
ENST00000639268.1:c.370C>G
ENST00000639341.1:c.260C>G
ENST00000639770.1:c.773C>G	ENSP00000491999.1:n.773C>G
ENST00000640390.1:n.665C>G
ENST00000640469.1:c.99C>G	ENSP00000491875.1:p.His33Gln
ENST00000640560.1:n.511C>G
ENST00000640893.1:c.*133C>G	ENSP00000492677.1:n.*133C>G
ENST00000262493.10:c.735C>G	ENSP00000262493.6:p.His245Gln
ENST00000568375.1:n.116-3471C>G
NM_020988.2:c.735C>G	NP_066268.1:p.His245Gln
XM_011523003.1:c.609C>G	XP_011521305.1:p.His203Gln
XM_011523003.3:c.609C>G	XP_011521305.1:p.His203Gln
NM_020988.3:c.735C>G MANE Select	NP_066268.1:p.His245Gln