Canonical Allele Identifier: CA395955342

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56388925T>C (hg19) ; chr16:g.56355013T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56355013T>C , CM000678.2:g.56355013T>C	GRCh38
NC_000016.9:g.56388925T>C , CM000678.1:g.56388925T>C	GRCh37
NC_000016.8:g.54946426T>C	NCBI36
NG_042800.1:g.168675T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.1025T>C MANE Select	ENSP00000262493.6:p.Ile342Thr
ENST00000562316.6:c.545-1090T>C	ENSP00000457238.2:n.545-1090T>C
ENST00000564727.2:c.303+26T>C	ENSP00000454971.2:n.303+26T>C
ENST00000568375.2:c.263T>C
ENST00000638210.1:n.1325T>C
ENST00000638705.1:c.1025T>C	ENSP00000491223.1:p.Ile342Thr
ENST00000638836.1:n.935T>C
ENST00000639251.1:n.926T>C
ENST00000639268.1:c.660T>C
ENST00000639341.1:c.550T>C
ENST00000639770.1:c.1063T>C	ENSP00000491999.1:n.1063T>C
ENST00000640390.1:n.955T>C
ENST00000640469.1:c.389T>C	ENSP00000491875.1:p.Ile130Thr
ENST00000640560.1:n.801T>C
ENST00000640893.1:c.*423T>C	ENSP00000492677.1:n.*423T>C
ENST00000262493.10:c.1025T>C	ENSP00000262493.6:p.Ile342Thr
ENST00000564727.1:c.245T>C	ENSP00000454971.1:p.Ile82Thr
ENST00000568375.1:n.263T>C
NM_020988.2:c.1025T>C	NP_066268.1:p.Ile342Thr
XM_011523003.1:c.899T>C	XP_011521305.1:p.Ile300Thr
XM_011523003.3:c.899T>C	XP_011521305.1:p.Ile300Thr
NM_020988.3:c.1025T>C MANE Select	NP_066268.1:p.Ile342Thr