Canonical Allele Identifier: CA2224108767
Gene: GNAO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56351531T= , CM000678.2:g.56351531T= GRCh38
NC_000016.9:g.56385443T= , CM000678.1:g.56385443T= GRCh37
NC_000016.8:g.54942944T= NCBI36
NG_042800.1:g.165193T=

Transcript Alleles

HGVS Amino-acid change
ENST00000262493.12:c.871T= MANE Select ENSP00000262493.6:p.Tyr291=
ENST00000562316.6:c.538T= ENSP00000457238.2:p.Tyr180=
ENST00000564727.2:c.175T= ENSP00000454971.2:p.Tyr59=
ENST00000568375.2:c.116-3335T=
ENST00000638185.1:n.1086T=
ENST00000638210.1:n.1171T=
ENST00000638705.1:c.871T= ENSP00000491223.1:p.Tyr291=
ENST00000638836.1:n.781T=
ENST00000639055.1:n.1592T=
ENST00000639251.1:n.772T=
ENST00000639268.1:c.506T=
ENST00000639341.1:c.396T=
ENST00000639770.1:c.909T= ENSP00000491999.1:n.909T=
ENST00000640390.1:n.801T=
ENST00000640469.1:c.235T= ENSP00000491875.1:p.Tyr79=
ENST00000640560.1:n.647T=
ENST00000640893.1:c.*269T= ENSP00000492677.1:n.*269T=
ENST00000262493.10:c.871T= ENSP00000262493.6:p.Tyr291=
ENST00000564727.1:c.91T= ENSP00000454971.1:p.Tyr31=
ENST00000568375.1:n.116-3335T=
NM_020988.2:c.871T= NP_066268.1:p.Tyr291=
XM_011523003.1:c.745T= XP_011521305.1:p.Tyr249=
XM_011523003.3:c.745T= XP_011521305.1:p.Tyr249=
NM_020988.3:c.871T= MANE Select NP_066268.1:p.Tyr291=