Canonical Allele Identifier: CA395954975

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56388790A>C (hg19) ; chr16:g.56354878A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56354878A>C , CM000678.2:g.56354878A>C	GRCh38
NC_000016.9:g.56388790A>C , CM000678.1:g.56388790A>C	GRCh37
NC_000016.8:g.54946291A>C	NCBI36
NG_042800.1:g.168540A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.890A>C MANE Select	ENSP00000262493.6:p.Tyr297Ser
ENST00000562316.6:c.545-1225A>C	ENSP00000457238.2:n.545-1225A>C
ENST00000564727.2:c.194A>C	ENSP00000454971.2:p.Tyr65Ser
ENST00000568375.2:c.128A>C
ENST00000638185.1:n.1105A>C
ENST00000638210.1:n.1190A>C
ENST00000638705.1:c.890A>C	ENSP00000491223.1:p.Tyr297Ser
ENST00000638836.1:n.800A>C
ENST00000639055.1:n.1611A>C
ENST00000639251.1:n.791A>C
ENST00000639268.1:c.525A>C
ENST00000639341.1:c.415A>C
ENST00000639770.1:c.928A>C	ENSP00000491999.1:n.928A>C
ENST00000640390.1:n.820A>C
ENST00000640469.1:c.254A>C	ENSP00000491875.1:p.Tyr85Ser
ENST00000640560.1:n.666A>C
ENST00000640893.1:c.*288A>C	ENSP00000492677.1:n.*288A>C
ENST00000262493.10:c.890A>C	ENSP00000262493.6:p.Tyr297Ser
ENST00000564727.1:c.110A>C	ENSP00000454971.1:p.Tyr37Ser
ENST00000568375.1:n.128A>C
NM_020988.2:c.890A>C	NP_066268.1:p.Tyr297Ser
XM_011523003.1:c.764A>C	XP_011521305.1:p.Tyr255Ser
XM_011523003.3:c.764A>C	XP_011521305.1:p.Tyr255Ser
NM_020988.3:c.890A>C MANE Select	NP_066268.1:p.Tyr297Ser