Canonical Allele Identifier: CA2633315196
Gene: GNAO1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56336908_56336912dup , CM000678.2:g.56336908_56336912dup GRCh38
NC_000016.9:g.56370820_56370824dup , CM000678.1:g.56370820_56370824dup GRCh37
NC_000016.8:g.54928321_54928325dup NCBI36
NG_042800.1:g.150570_150574dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000262494.13:c.723+48_723+52dup ENSP00000262494.7:n.723+48_723+52dup
ENST00000262493.12:c.723+48_723+52dup MANE Select ENSP00000262493.6:n.723+48_723+52dup
ENST00000262494.12:c.723+48_723+52dup ENSP00000262494.7:n.723+48_723+52dup
ENST00000562316.6:c.390+48_390+52dup ENSP00000457238.2:n.390+48_390+52dup
ENST00000564727.2:c.27+48_27+52dup ENSP00000454971.2:n.27+48_27+52dup
ENST00000568375.2:c.115+48_115+52dup
ENST00000638185.1:n.938+48_938+52dup
ENST00000638210.1:n.1023+48_1023+52dup
ENST00000638705.1:c.723+48_723+52dup ENSP00000491223.1:n.723+48_723+52dup
ENST00000638836.1:n.633+48_633+52dup
ENST00000639055.1:n.1444+48_1444+52dup
ENST00000639251.1:n.624+48_624+52dup
ENST00000639268.1:c.358+48_358+52dup
ENST00000639341.1:c.248+48_248+52dup
ENST00000639770.1:c.761+48_761+52dup ENSP00000491999.1:n.761+48_761+52dup
ENST00000640390.1:n.653+48_653+52dup
ENST00000640469.1:c.87+48_87+52dup ENSP00000491875.1:n.87+48_87+52dup
ENST00000640560.1:n.499+48_499+52dup
ENST00000640893.1:c.*121+48_*121+52dup ENSP00000492677.1:n.*121+48_*121+52dup
ENST00000262493.10:c.723+48_723+52dup ENSP00000262493.6:n.723+48_723+52dup
ENST00000262494.11:c.723+48_723+52dup ENSP00000262494.7:n.723+48_723+52dup
ENST00000568375.1:n.115+48_115+52dup
NM_020988.2:c.723+48_723+52dup NP_066268.1:n.723+48_723+52dup
NM_138736.2:c.723+48_723+52dup NP_620073.2:n.723+48_723+52dup
XM_011523003.1:c.597+48_597+52dup XP_011521305.1:n.597+48_597+52dup
XM_011523003.3:c.597+48_597+52dup XP_011521305.1:n.597+48_597+52dup
NM_020988.3:c.723+48_723+52dup MANE Select NP_066268.1:n.723+48_723+52dup
NM_138736.3:c.723+48_723+52dup NP_620073.2:n.723+48_723+52dup