Canonical Allele Identifier: CA2633315070
Gene: GNAO1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56336646T>C , CM000678.2:g.56336646T>C GRCh38
NC_000016.9:g.56370558T>C , CM000678.1:g.56370558T>C GRCh37
NC_000016.8:g.54928059T>C NCBI36
NG_042800.1:g.150308T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262494.13:c.594-85T>C ENSP00000262494.7:n.594-85T>C
ENST00000262493.12:c.594-85T>C MANE Select ENSP00000262493.6:n.594-85T>C
ENST00000262494.12:c.594-85T>C ENSP00000262494.7:n.594-85T>C
ENST00000562316.6:c.261-85T>C ENSP00000457238.2:n.261-85T>C
ENST00000638185.1:n.809-85T>C
ENST00000638210.1:n.894-85T>C
ENST00000638705.1:c.594-85T>C ENSP00000491223.1:n.594-85T>C
ENST00000638836.1:n.504-85T>C
ENST00000639055.1:n.1315-85T>C
ENST00000639251.1:n.495-85T>C
ENST00000639268.1:c.229-85T>C
ENST00000639341.1:c.119-85T>C
ENST00000639770.1:c.632-85T>C ENSP00000491999.1:n.632-85T>C
ENST00000640390.1:n.524-85T>C
ENST00000640560.1:n.285T>C
ENST00000640893.1:c.433-85T>C ENSP00000492677.1:n.433-85T>C
ENST00000262493.10:c.594-85T>C ENSP00000262493.6:n.594-85T>C
ENST00000262494.11:c.594-85T>C ENSP00000262494.7:n.594-85T>C
NM_020988.2:c.594-85T>C NP_066268.1:n.594-85T>C
NM_138736.2:c.594-85T>C NP_620073.2:n.594-85T>C
XM_011523003.1:c.468-85T>C XP_011521305.1:n.468-85T>C
XM_011523003.3:c.468-85T>C XP_011521305.1:n.468-85T>C
NM_020988.3:c.594-85T>C MANE Select NP_066268.1:n.594-85T>C
NM_138736.3:c.594-85T>C NP_620073.2:n.594-85T>C