Canonical Allele Identifier: CA395952237

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56370690A>C (hg19) ; chr16:g.56336778A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336778A>C , CM000678.2:g.56336778A>C	GRCh38
NC_000016.9:g.56370690A>C , CM000678.1:g.56370690A>C	GRCh37
NC_000016.8:g.54928191A>C	NCBI36
NG_042800.1:g.150440A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.641A>C	ENSP00000262494.7:p.His214Pro
ENST00000262493.12:c.641A>C MANE Select	ENSP00000262493.6:p.His214Pro
ENST00000262494.12:c.641A>C	ENSP00000262494.7:p.His214Pro
ENST00000562316.6:c.308A>C	ENSP00000457238.2:p.His103Pro
ENST00000568375.2:c.33A>C
ENST00000638185.1:n.856A>C
ENST00000638210.1:n.941A>C
ENST00000638705.1:c.641A>C	ENSP00000491223.1:p.His214Pro
ENST00000638836.1:n.551A>C
ENST00000639055.1:n.1362A>C
ENST00000639251.1:n.542A>C
ENST00000639268.1:c.276A>C
ENST00000639341.1:c.166A>C
ENST00000639770.1:c.679A>C	ENSP00000491999.1:n.679A>C
ENST00000640390.1:n.571A>C
ENST00000640469.1:c.5A>C	ENSP00000491875.1:p.His2Pro
ENST00000640560.1:n.417A>C
ENST00000640893.1:c.*39A>C	ENSP00000492677.1:n.*39A>C
ENST00000262493.10:c.641A>C	ENSP00000262493.6:p.His214Pro
ENST00000262494.11:c.641A>C	ENSP00000262494.7:p.His214Pro
ENST00000568375.1:n.33A>C
NM_020988.2:c.641A>C	NP_066268.1:p.His214Pro
NM_138736.2:c.641A>C	NP_620073.2:p.His214Pro
XM_011523003.1:c.515A>C	XP_011521305.1:p.His172Pro
XM_011523003.3:c.515A>C	XP_011521305.1:p.His172Pro
NM_020988.3:c.641A>C MANE Select	NP_066268.1:p.His214Pro
NM_138736.3:c.641A>C	NP_620073.2:p.His214Pro