Canonical Allele Identifier: CA2840732404
Gene: GNAO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56336865G>T , CM000678.2:g.56336865G>T GRCh38
NC_000016.9:g.56370777G>T , CM000678.1:g.56370777G>T GRCh37
NC_000016.8:g.54928278G>T NCBI36
NG_042800.1:g.150527G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262494.13:c.723+5G>T ENSP00000262494.7:n.723+5G>T
ENST00000262493.12:c.723+5G>T MANE Select ENSP00000262493.6:n.723+5G>T
ENST00000262494.12:c.723+5G>T ENSP00000262494.7:n.723+5G>T
ENST00000562316.6:c.390+5G>T ENSP00000457238.2:n.390+5G>T
ENST00000564727.2:c.27+5G>T ENSP00000454971.2:n.27+5G>T
ENST00000568375.2:c.115+5G>T
ENST00000638185.1:n.938+5G>T
ENST00000638210.1:n.1023+5G>T
ENST00000638705.1:c.723+5G>T ENSP00000491223.1:n.723+5G>T
ENST00000638836.1:n.633+5G>T
ENST00000639055.1:n.1444+5G>T
ENST00000639251.1:n.624+5G>T
ENST00000639268.1:c.358+5G>T
ENST00000639341.1:c.248+5G>T
ENST00000639770.1:c.761+5G>T ENSP00000491999.1:n.761+5G>T
ENST00000640390.1:n.653+5G>T
ENST00000640469.1:c.87+5G>T ENSP00000491875.1:n.87+5G>T
ENST00000640560.1:n.499+5G>T
ENST00000640893.1:c.*121+5G>T ENSP00000492677.1:n.*121+5G>T
ENST00000262493.10:c.723+5G>T ENSP00000262493.6:n.723+5G>T
ENST00000262494.11:c.723+5G>T ENSP00000262494.7:n.723+5G>T
ENST00000568375.1:n.115+5G>T
NM_020988.2:c.723+5G>T NP_066268.1:n.723+5G>T
NM_138736.2:c.723+5G>T NP_620073.2:n.723+5G>T
XM_011523003.1:c.597+5G>T XP_011521305.1:n.597+5G>T
XM_011523003.3:c.597+5G>T XP_011521305.1:n.597+5G>T
NM_020988.3:c.723+5G>T MANE Select NP_066268.1:n.723+5G>T
NM_138736.3:c.723+5G>T NP_620073.2:n.723+5G>T