Canonical Allele Identifier: CA8064005
Gene: GNAO1 HGNC NCBI

Linked Data

dbSNP Id: rs781523996

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56351566del , CM000678.2:g.56351566del GRCh38
NC_000016.9:g.56385478del , CM000678.1:g.56385478del GRCh37
NC_000016.8:g.54942979del NCBI36
NG_042800.1:g.165228del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262493.12:c.877+29del MANE Select ENSP00000262493.6:n.877+29del
ENST00000562316.6:c.544+29del ENSP00000457238.2:n.544+29del
ENST00000564727.2:c.181+29del ENSP00000454971.2:n.181+29del
ENST00000568375.2:c.116-3300del
ENST00000638185.1:n.1092+29del
ENST00000638210.1:n.1177+29del
ENST00000638705.1:c.877+29del ENSP00000491223.1:n.877+29del
ENST00000638836.1:n.787+29del
ENST00000639055.1:n.1598+29del
ENST00000639251.1:n.778+29del
ENST00000639268.1:c.512+29del
ENST00000639341.1:c.402+29del
ENST00000639770.1:c.915+29del ENSP00000491999.1:n.915+29del
ENST00000640390.1:n.807+29del
ENST00000640469.1:c.241+29del ENSP00000491875.1:n.241+29del
ENST00000640560.1:n.653+29del
ENST00000640893.1:c.*275+29del ENSP00000492677.1:n.*275+29del
ENST00000262493.10:c.877+29del ENSP00000262493.6:n.877+29del
ENST00000564727.1:c.97+29del ENSP00000454971.1:n.97+29del
ENST00000568375.1:n.116-3300del
NM_020988.2:c.877+29del NP_066268.1:n.877+29del
XM_011523003.1:c.751+29del XP_011521305.1:n.751+29del
XM_011523003.3:c.751+29del XP_011521305.1:n.751+29del
NM_020988.3:c.877+29del MANE Select NP_066268.1:n.877+29del