Canonical Allele Identifier: CA2575998584
Gene: GNAO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56351541_56351544del , CM000678.2:g.56351541_56351544del GRCh38
NC_000016.9:g.56385453_56385456del , CM000678.1:g.56385453_56385456del GRCh37
NC_000016.8:g.54942954_54942957del NCBI36
NG_042800.1:g.165203_165206del

Transcript Alleles

HGVS Amino-acid change
ENST00000262493.12:c.877+4_877+7del
ENST00000562316.6:c.544+4_544+7del
ENST00000564727.2:c.181+4_181+7del
ENST00000568375.2:c.116-3325_116-3322del
ENST00000638185.1:n.1092+4_1092+7del
ENST00000638210.1:n.1177+4_1177+7del
ENST00000638705.1:c.877+4_877+7del
ENST00000638836.1:n.787+4_787+7del
ENST00000639055.1:n.1598+4_1598+7del
ENST00000639251.1:n.778+4_778+7del
ENST00000639268.1:c.512+4_512+7del
ENST00000639341.1:c.402+4_402+7del
ENST00000639770.1:c.915+4_915+7del
ENST00000640390.1:n.807+4_807+7del
ENST00000640469.1:c.241+4_241+7del
ENST00000640560.1:n.653+4_653+7del
ENST00000640893.1:c.*275+4_*275+7del
ENST00000262493.10:c.877+4_877+7del
ENST00000564727.1:c.97+4_97+7del
ENST00000568375.1:n.116-3325_116-3322del
NM_020988.2:c.877+4_877+7del
XM_011523003.1:c.751+4_751+7del
XM_011523003.3:c.751+4_751+7del
NM_020988.3:c.877+4_877+7del