Canonical Allele Identifier: CA1857429038

Gene: GNAQ

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.77794117_77794118delinsAC , CM000671.2:g.77794117_77794118delinsAC	GRCh38
NC_000009.11:g.80409033_80409034delinsAC , CM000671.1:g.80409033_80409034delinsAC	GRCh37
NC_000009.10:g.79598853_79598854delinsAC	NCBI36
NG_027904.2:g.242186_242187delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286548.9:c.735+345_735+346delinsGT MANE Select	ENSP00000286548.4:n.735+345_735+346delinsGT
ENST00000286548.8:c.735+345_735+346delinsGT	ENSP00000286548.4:n.735+345_735+346delinsGT
NM_002072.4:c.735+345_735+346delinsGT	NP_002063.2:n.735+345_735+346delinsGT
XM_017014628.2:c.561+345_561+346delinsGT	XP_016870117.1:n.561+345_561+346delinsGT
NM_002072.5:c.735+345_735+346delinsGT MANE Select	NP_002063.2:n.735+345_735+346delinsGT