Canonical Allele Identifier: CA2633321924

Gene: GNAO1

Linked Data

• gnomAD v4: 16-56351529-A-AATACACAGGTGGGTGCCAGGCAGTCCTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351530_56351558dup , CM000678.2:g.56351530_56351558dup	GRCh38
NC_000016.9:g.56385442_56385470dup , CM000678.1:g.56385442_56385470dup	GRCh37
NC_000016.8:g.54942943_54942971dup	NCBI36
NG_042800.1:g.165192_165220dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000262493.12:c.870_877+21dup
ENST00000562316.6:c.537_544+21dup
ENST00000564727.2:c.174_181+21dup
ENST00000568375.2:c.116-3336_116-3308dup
ENST00000638185.1:n.1085_1092+21dup
ENST00000638210.1:n.1170_1177+21dup
ENST00000638705.1:c.870_877+21dup
ENST00000638836.1:n.780_787+21dup
ENST00000639055.1:n.1591_1598+21dup
ENST00000639251.1:n.771_778+21dup
ENST00000639268.1:c.505_512+21dup
ENST00000639341.1:c.395_402+21dup
ENST00000639770.1:c.908_915+21dup
ENST00000640390.1:n.800_807+21dup
ENST00000640469.1:c.234_241+21dup
ENST00000640560.1:n.646_653+21dup
ENST00000640893.1:c.*268_*275+21dup
ENST00000262493.10:c.870_877+21dup
ENST00000564727.1:c.90_97+21dup
ENST00000568375.1:n.116-3336_116-3308dup
NM_020988.2:c.870_877+21dup
XM_011523003.1:c.744_751+21dup
XM_011523003.3:c.744_751+21dup
NM_020988.3:c.870_877+21dup