Canonical Allele Identifier: CA395952277

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56370705T>A (hg19) ; chr16:g.56336793T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336793T>A , CM000678.2:g.56336793T>A	GRCh38
NC_000016.9:g.56370705T>A , CM000678.1:g.56370705T>A	GRCh37
NC_000016.8:g.54928206T>A	NCBI36
NG_042800.1:g.150455T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.656T>A	ENSP00000262494.7:p.Val219Asp
ENST00000262493.12:c.656T>A MANE Select	ENSP00000262493.6:p.Val219Asp
ENST00000262494.12:c.656T>A	ENSP00000262494.7:p.Val219Asp
ENST00000562316.6:c.323T>A	ENSP00000457238.2:p.Val108Asp
ENST00000568375.2:c.48T>A
ENST00000638185.1:n.871T>A
ENST00000638210.1:n.956T>A
ENST00000638705.1:c.656T>A	ENSP00000491223.1:p.Val219Asp
ENST00000638836.1:n.566T>A
ENST00000639055.1:n.1377T>A
ENST00000639251.1:n.557T>A
ENST00000639268.1:c.291T>A
ENST00000639341.1:c.181T>A
ENST00000639770.1:c.694T>A	ENSP00000491999.1:n.694T>A
ENST00000640390.1:n.586T>A
ENST00000640469.1:c.20T>A	ENSP00000491875.1:p.Val7Asp
ENST00000640560.1:n.432T>A
ENST00000640893.1:c.*54T>A	ENSP00000492677.1:n.*54T>A
ENST00000262493.10:c.656T>A	ENSP00000262493.6:p.Val219Asp
ENST00000262494.11:c.656T>A	ENSP00000262494.7:p.Val219Asp
ENST00000568375.1:n.48T>A
NM_020988.2:c.656T>A	NP_066268.1:p.Val219Asp
NM_138736.2:c.656T>A	NP_620073.2:p.Val219Asp
XM_011523003.1:c.530T>A	XP_011521305.1:p.Val177Asp
XM_011523003.3:c.530T>A	XP_011521305.1:p.Val177Asp
NM_020988.3:c.656T>A MANE Select	NP_066268.1:p.Val219Asp
NM_138736.3:c.656T>A	NP_620073.2:p.Val219Asp