Canonical Allele Identifier: CA1857429024

Gene: GNAQ

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.77794103_77794108delinsGAAAAC , CM000671.2:g.77794103_77794108delinsGAAAAC	GRCh38
NC_000009.11:g.80409019_80409024delinsGAAAAC , CM000671.1:g.80409019_80409024delinsGAAAAC	GRCh37
NC_000009.10:g.79598839_79598844delinsGAAAAC	NCBI36
NG_027904.2:g.242196_242201delinsGTTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286548.9:c.735+355_735+360delinsGTTTTC MANE Select	ENSP00000286548.4:n.735+355_735+360delinsGTTTTC
ENST00000286548.8:c.735+355_735+360delinsGTTTTC	ENSP00000286548.4:n.735+355_735+360delinsGTTTTC
NM_002072.4:c.735+355_735+360delinsGTTTTC	NP_002063.2:n.735+355_735+360delinsGTTTTC
XM_017014628.2:c.561+355_561+360delinsGTTTTC	XP_016870117.1:n.561+355_561+360delinsGTTTTC
NM_002072.5:c.735+355_735+360delinsGTTTTC MANE Select	NP_002063.2:n.735+355_735+360delinsGTTTTC