Canonical Allele Identifier: CA2224108809
Gene: GNAO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56351640A= , CM000678.2:g.56351640A= GRCh38
NC_000016.9:g.56385552A= , CM000678.1:g.56385552A= GRCh37
NC_000016.8:g.54943053A= NCBI36
NG_042800.1:g.165302A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262493.12:c.877+103A= MANE Select ENSP00000262493.6:n.877+103A=
ENST00000562316.6:c.544+103A= ENSP00000457238.2:n.544+103A=
ENST00000564727.2:c.181+103A= ENSP00000454971.2:n.181+103A=
ENST00000568375.2:c.116-3226A=
ENST00000638185.1:n.1092+103A=
ENST00000638210.1:n.1177+103A=
ENST00000638705.1:c.877+103A= ENSP00000491223.1:n.877+103A=
ENST00000638836.1:n.787+103A=
ENST00000639055.1:n.1598+103A=
ENST00000639251.1:n.778+103A=
ENST00000639268.1:c.512+103A=
ENST00000639341.1:c.402+103A=
ENST00000639770.1:c.915+103A= ENSP00000491999.1:n.915+103A=
ENST00000640390.1:n.807+103A=
ENST00000640469.1:c.241+103A= ENSP00000491875.1:n.241+103A=
ENST00000640560.1:n.653+103A=
ENST00000640893.1:c.*275+103A= ENSP00000492677.1:n.*275+103A=
ENST00000262493.10:c.877+103A= ENSP00000262493.6:n.877+103A=
ENST00000564727.1:c.97+103A= ENSP00000454971.1:n.97+103A=
ENST00000568375.1:n.116-3226A=
NM_020988.2:c.877+103A= NP_066268.1:n.877+103A=
XM_011523003.1:c.751+103A= XP_011521305.1:n.751+103A=
XM_011523003.3:c.751+103A= XP_011521305.1:n.751+103A=
NM_020988.3:c.877+103A= MANE Select NP_066268.1:n.877+103A=