Canonical Allele Identifier: CA2633321932

Gene: GNAO1

Linked Data

• gnomAD v4: 16-56351546-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351546C>T , CM000678.2:g.56351546C>T	GRCh38
NC_000016.9:g.56385458C>T , CM000678.1:g.56385458C>T	GRCh37
NC_000016.8:g.54942959C>T	NCBI36
NG_042800.1:g.165208C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262493.12:c.877+9C>T MANE Select	ENSP00000262493.6:n.877+9C>T
ENST00000562316.6:c.544+9C>T	ENSP00000457238.2:n.544+9C>T
ENST00000564727.2:c.181+9C>T	ENSP00000454971.2:n.181+9C>T
ENST00000568375.2:c.116-3320C>T
ENST00000638185.1:n.1092+9C>T
ENST00000638210.1:n.1177+9C>T
ENST00000638705.1:c.877+9C>T	ENSP00000491223.1:n.877+9C>T
ENST00000638836.1:n.787+9C>T
ENST00000639055.1:n.1598+9C>T
ENST00000639251.1:n.778+9C>T
ENST00000639268.1:c.512+9C>T
ENST00000639341.1:c.402+9C>T
ENST00000639770.1:c.915+9C>T	ENSP00000491999.1:n.915+9C>T
ENST00000640390.1:n.807+9C>T
ENST00000640469.1:c.241+9C>T	ENSP00000491875.1:n.241+9C>T
ENST00000640560.1:n.653+9C>T
ENST00000640893.1:c.*275+9C>T	ENSP00000492677.1:n.*275+9C>T
ENST00000262493.10:c.877+9C>T	ENSP00000262493.6:n.877+9C>T
ENST00000564727.1:c.97+9C>T	ENSP00000454971.1:n.97+9C>T
ENST00000568375.1:n.116-3320C>T
NM_020988.2:c.877+9C>T	NP_066268.1:n.877+9C>T
XM_011523003.1:c.751+9C>T	XP_011521305.1:n.751+9C>T
XM_011523003.3:c.751+9C>T	XP_011521305.1:n.751+9C>T
NM_020988.3:c.877+9C>T MANE Select	NP_066268.1:n.877+9C>T