Canonical Allele Identifier: CA658658473

Gene: GNAO1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56276078C>T , CM000678.2:g.56276078C>T	GRCh38
NC_000016.9:g.56309990C>T , CM000678.1:g.56309990C>T	GRCh37
NC_000016.8:g.54867491C>T	NCBI36
NG_042800.1:g.89740C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.303+6C>T	ENSP00000262494.7:n.303+6C>T
ENST00000262493.12:c.303+6C>T MANE Select	ENSP00000262493.6:n.303+6C>T
ENST00000262494.12:c.303+6C>T	ENSP00000262494.7:n.303+6C>T
ENST00000563661.2:c.309C>T	ENSP00000492694.1:p.Gly103=
ENST00000638185.1:n.518+6C>T
ENST00000638210.1:n.603+6C>T
ENST00000638705.1:c.303+6C>T	ENSP00000491223.1:n.303+6C>T
ENST00000638836.1:n.213+6C>T
ENST00000639055.1:n.1024+6C>T
ENST00000639251.1:n.204+6C>T
ENST00000639268.1:c.67+6C>T
ENST00000639770.1:c.341+6C>T	ENSP00000491999.1:n.341+6C>T
ENST00000639966.1:n.318+6C>T
ENST00000640390.1:n.233+6C>T
ENST00000640893.1:c.303+6C>T	ENSP00000492677.1:n.303+6C>T
ENST00000262493.10:c.303+6C>T	ENSP00000262493.6:n.303+6C>T
ENST00000262494.11:c.303+6C>T	ENSP00000262494.7:n.303+6C>T
ENST00000562316.5:c.42+6C>T	ENSP00000457238.1:n.42+6C>T
ENST00000563440.1:c.42+6C>T	ENSP00000455774.1:n.42+6C>T
ENST00000563661.1:n.306C>T
ENST00000565363.5:c.177+6C>T	ENSP00000454728.1:n.177+6C>T
NM_020988.2:c.303+6C>T	NP_066268.1:n.303+6C>T
NM_138736.2:c.303+6C>T	NP_620073.2:n.303+6C>T
XM_011523003.1:c.177+6C>T	XP_011521305.1:n.177+6C>T
XM_011523003.3:c.177+6C>T	XP_011521305.1:n.177+6C>T
NM_020988.3:c.303+6C>T MANE Select	NP_066268.1:n.303+6C>T
NM_138736.3:c.303+6C>T	NP_620073.2:n.303+6C>T