Canonical Allele Identifier: CA395952292

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56370713A>T (hg19) ; chr16:g.56336801A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336801A>T , CM000678.2:g.56336801A>T	GRCh38
NC_000016.9:g.56370713A>T , CM000678.1:g.56370713A>T	GRCh37
NC_000016.8:g.54928214A>T	NCBI36
NG_042800.1:g.150463A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.664A>T	ENSP00000262494.7:p.Ile222Phe
ENST00000262493.12:c.664A>T MANE Select	ENSP00000262493.6:p.Ile222Phe
ENST00000262494.12:c.664A>T	ENSP00000262494.7:p.Ile222Phe
ENST00000562316.6:c.331A>T	ENSP00000457238.2:p.Ile111Phe
ENST00000568375.2:c.56A>T
ENST00000638185.1:n.879A>T
ENST00000638210.1:n.964A>T
ENST00000638705.1:c.664A>T	ENSP00000491223.1:p.Ile222Phe
ENST00000638836.1:n.574A>T
ENST00000639055.1:n.1385A>T
ENST00000639251.1:n.565A>T
ENST00000639268.1:c.299A>T
ENST00000639341.1:c.189A>T
ENST00000639770.1:c.702A>T	ENSP00000491999.1:n.702A>T
ENST00000640390.1:n.594A>T
ENST00000640469.1:c.28A>T	ENSP00000491875.1:p.Ile10Phe
ENST00000640560.1:n.440A>T
ENST00000640893.1:c.*62A>T	ENSP00000492677.1:n.*62A>T
ENST00000262493.10:c.664A>T	ENSP00000262493.6:p.Ile222Phe
ENST00000262494.11:c.664A>T	ENSP00000262494.7:p.Ile222Phe
ENST00000568375.1:n.56A>T
NM_020988.2:c.664A>T	NP_066268.1:p.Ile222Phe
NM_138736.2:c.664A>T	NP_620073.2:p.Ile222Phe
XM_011523003.1:c.538A>T	XP_011521305.1:p.Ile180Phe
XM_011523003.3:c.538A>T	XP_011521305.1:p.Ile180Phe
NM_020988.3:c.664A>T MANE Select	NP_066268.1:p.Ile222Phe
NM_138736.3:c.664A>T	NP_620073.2:p.Ile222Phe