Canonical Allele Identifier: CA2224108775
Gene: GNAO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56351561_56351562delinsAG , CM000678.2:g.56351561_56351562delinsAG GRCh38
NC_000016.9:g.56385473_56385474delinsAG , CM000678.1:g.56385473_56385474delinsAG GRCh37
NC_000016.8:g.54942974_54942975delinsAG NCBI36
NG_042800.1:g.165223_165224delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000262493.12:c.877+24_877+25delinsAG MANE Select ENSP00000262493.6:n.877+24_877+25delinsAG
ENST00000562316.6:c.544+24_544+25delinsAG ENSP00000457238.2:n.544+24_544+25delinsAG
ENST00000564727.2:c.181+24_181+25delinsAG ENSP00000454971.2:n.181+24_181+25delinsAG
ENST00000568375.2:c.116-3305_116-3304delinsAG
ENST00000638185.1:n.1092+24_1092+25delinsAG
ENST00000638210.1:n.1177+24_1177+25delinsAG
ENST00000638705.1:c.877+24_877+25delinsAG ENSP00000491223.1:n.877+24_877+25delinsAG
ENST00000638836.1:n.787+24_787+25delinsAG
ENST00000639055.1:n.1598+24_1598+25delinsAG
ENST00000639251.1:n.778+24_778+25delinsAG
ENST00000639268.1:c.512+24_512+25delinsAG
ENST00000639341.1:c.402+24_402+25delinsAG
ENST00000639770.1:c.915+24_915+25delinsAG ENSP00000491999.1:n.915+24_915+25delinsAG
ENST00000640390.1:n.807+24_807+25delinsAG
ENST00000640469.1:c.241+24_241+25delinsAG ENSP00000491875.1:n.241+24_241+25delinsAG
ENST00000640560.1:n.653+24_653+25delinsAG
ENST00000640893.1:c.*275+24_*275+25delinsAG ENSP00000492677.1:n.*275+24_*275+25delinsAG
ENST00000262493.10:c.877+24_877+25delinsAG ENSP00000262493.6:n.877+24_877+25delinsAG
ENST00000564727.1:c.97+24_97+25delinsAG ENSP00000454971.1:n.97+24_97+25delinsAG
ENST00000568375.1:n.116-3305_116-3304delinsAG
NM_020988.2:c.877+24_877+25delinsAG NP_066268.1:n.877+24_877+25delinsAG
XM_011523003.1:c.751+24_751+25delinsAG XP_011521305.1:n.751+24_751+25delinsAG
XM_011523003.3:c.751+24_751+25delinsAG XP_011521305.1:n.751+24_751+25delinsAG
NM_020988.3:c.877+24_877+25delinsAG MANE Select NP_066268.1:n.877+24_877+25delinsAG