Canonical Allele Identifier: CA2784733716

Gene: GNAQ

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.77794647_77794648insCAACCAAACACACCCAAC , CM000671.2:g.77794647_77794648insCAACCAAACACACCCAAC	GRCh38
NC_000009.11:g.80409563_80409564insCAACCAAACACACCCAAC , CM000671.1:g.80409563_80409564insCAACCAAACACACCCAAC	GRCh37
NC_000009.10:g.79599383_79599384insCAACCAAACACACCCAAC	NCBI36
NG_027904.2:g.241656_241657insGTTGGGTGTGTTTGGTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286548.9:c.606-56_606-55insGTTGGGTGTGTTTGGTTG MANE Select	ENSP00000286548.4:n.606-56_606-55insGTTGGGTGTGTTTGGTTG
ENST00000286548.8:c.606-56_606-55insGTTGGGTGTGTTTGGTTG	ENSP00000286548.4:n.606-56_606-55insGTTGGGTGTGTTTGGTTG
NM_002072.4:c.606-56_606-55insGTTGGGTGTGTTTGGTTG	NP_002063.2:n.606-56_606-55insGTTGGGTGTGTTTGGTTG
XM_017014628.2:c.432-56_432-55insGTTGGGTGTGTTTGGTTG	XP_016870117.1:n.432-56_432-55insGTTGGGTGTGTTTGGTTG
NM_002072.5:c.606-56_606-55insGTTGGGTGTGTTTGGTTG MANE Select	NP_002063.2:n.606-56_606-55insGTTGGGTGTGTTTGGTTG