Canonical Allele Identifier: CA395951577

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56368715T>A (hg19) ; chr16:g.56334803T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56334803T>A , CM000678.2:g.56334803T>A	GRCh38
NC_000016.9:g.56368715T>A , CM000678.1:g.56368715T>A	GRCh37
NC_000016.8:g.54926216T>A	NCBI36
NG_042800.1:g.148465T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.539T>A	ENSP00000262494.7:p.Val180Asp
ENST00000262493.12:c.539T>A MANE Select	ENSP00000262493.6:p.Val180Asp
ENST00000262494.12:c.539T>A	ENSP00000262494.7:p.Val180Asp
ENST00000562316.6:c.206T>A	ENSP00000457238.2:p.Val69Asp
ENST00000638185.1:n.754T>A
ENST00000638210.1:n.839T>A
ENST00000638705.1:c.539T>A	ENSP00000491223.1:p.Val180Asp
ENST00000638836.1:n.449T>A
ENST00000639055.1:n.1260T>A
ENST00000639251.1:n.440T>A
ENST00000639268.1:c.229-1928T>A
ENST00000639341.1:c.64T>A
ENST00000639770.1:c.577T>A	ENSP00000491999.1:n.577T>A
ENST00000640390.1:n.469T>A
ENST00000640893.1:c.378T>A	ENSP00000492677.1:p.Gly126=
ENST00000262493.10:c.539T>A	ENSP00000262493.6:p.Val180Asp
ENST00000262494.11:c.539T>A	ENSP00000262494.7:p.Val180Asp
ENST00000562316.5:c.278T>A	ENSP00000457238.1:p.Val93Asp
NM_020988.2:c.539T>A	NP_066268.1:p.Val180Asp
NM_138736.2:c.539T>A	NP_620073.2:p.Val180Asp
XM_011523003.1:c.413T>A	XP_011521305.1:p.Val138Asp
XM_011523003.3:c.413T>A	XP_011521305.1:p.Val138Asp
NM_020988.3:c.539T>A MANE Select	NP_066268.1:p.Val180Asp
NM_138736.3:c.539T>A	NP_620073.2:p.Val180Asp