Canonical Allele Identifier: CA395952246

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56370693G>C (hg19) ; chr16:g.56336781G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336781G>C , CM000678.2:g.56336781G>C	GRCh38
NC_000016.9:g.56370693G>C , CM000678.1:g.56370693G>C	GRCh37
NC_000016.8:g.54928194G>C	NCBI36
NG_042800.1:g.150443G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.644G>C	ENSP00000262494.7:p.Cys215Ser
ENST00000262493.12:c.644G>C MANE Select	ENSP00000262493.6:p.Cys215Ser
ENST00000262494.12:c.644G>C	ENSP00000262494.7:p.Cys215Ser
ENST00000562316.6:c.311G>C	ENSP00000457238.2:p.Cys104Ser
ENST00000568375.2:c.36G>C
ENST00000638185.1:n.859G>C
ENST00000638210.1:n.944G>C
ENST00000638705.1:c.644G>C	ENSP00000491223.1:p.Cys215Ser
ENST00000638836.1:n.554G>C
ENST00000639055.1:n.1365G>C
ENST00000639251.1:n.545G>C
ENST00000639268.1:c.279G>C
ENST00000639341.1:c.169G>C
ENST00000639770.1:c.682G>C	ENSP00000491999.1:n.682G>C
ENST00000640390.1:n.574G>C
ENST00000640469.1:c.8G>C	ENSP00000491875.1:p.Cys3Ser
ENST00000640560.1:n.420G>C
ENST00000640893.1:c.*42G>C	ENSP00000492677.1:n.*42G>C
ENST00000262493.10:c.644G>C	ENSP00000262493.6:p.Cys215Ser
ENST00000262494.11:c.644G>C	ENSP00000262494.7:p.Cys215Ser
ENST00000568375.1:n.36G>C
NM_020988.2:c.644G>C	NP_066268.1:p.Cys215Ser
NM_138736.2:c.644G>C	NP_620073.2:p.Cys215Ser
XM_011523003.1:c.518G>C	XP_011521305.1:p.Cys173Ser
XM_011523003.3:c.518G>C	XP_011521305.1:p.Cys173Ser
NM_020988.3:c.644G>C MANE Select	NP_066268.1:p.Cys215Ser
NM_138736.3:c.644G>C	NP_620073.2:p.Cys215Ser