Canonical Allele Identifier: CA2224102488
Gene: GNAO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56336743C= , CM000678.2:g.56336743C= GRCh38
NC_000016.9:g.56370655C= , CM000678.1:g.56370655C= GRCh37
NC_000016.8:g.54928156C= NCBI36
NG_042800.1:g.150405C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262494.13:c.606C= ENSP00000262494.7:p.Val202=
ENST00000262493.12:c.606C= MANE Select ENSP00000262493.6:p.Val202=
ENST00000262494.12:c.606C= ENSP00000262494.7:p.Val202=
ENST00000562316.6:c.273C= ENSP00000457238.2:p.Val91=
ENST00000638185.1:n.821C=
ENST00000638210.1:n.906C=
ENST00000638705.1:c.606C= ENSP00000491223.1:p.Val202=
ENST00000638836.1:n.516C=
ENST00000639055.1:n.1327C=
ENST00000639251.1:n.507C=
ENST00000639268.1:c.241C=
ENST00000639341.1:c.131C=
ENST00000639770.1:c.644C= ENSP00000491999.1:n.644C=
ENST00000640390.1:n.536C=
ENST00000640560.1:n.382C=
ENST00000640893.1:c.*4C= ENSP00000492677.1:n.*4C=
ENST00000262493.10:c.606C= ENSP00000262493.6:p.Val202=
ENST00000262494.11:c.606C= ENSP00000262494.7:p.Val202=
NM_020988.2:c.606C= NP_066268.1:p.Val202=
NM_138736.2:c.606C= NP_620073.2:p.Val202=
XM_011523003.1:c.480C= XP_011521305.1:p.Val160=
XM_011523003.3:c.480C= XP_011521305.1:p.Val160=
NM_020988.3:c.606C= MANE Select NP_066268.1:p.Val202=
NM_138736.3:c.606C= NP_620073.2:p.Val202=