Canonical Allele Identifier: CA2690385222

Gene: GNAQ

Linked Data

• gnomAD v4: 9-77794672-A-ATTTTTGTACCTAAAC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.77794672_77794673insTTTTTGTACCTAAAC , CM000671.2:g.77794672_77794673insTTTTTGTACCTAAAC	GRCh38
NC_000009.11:g.80409588_80409589insTTTTTGTACCTAAAC , CM000671.1:g.80409588_80409589insTTTTTGTACCTAAAC	GRCh37
NC_000009.10:g.79599408_79599409insTTTTTGTACCTAAAC	NCBI36
NG_027904.2:g.241631_241632insGTTTAGGTACAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286548.9:c.606-81_606-80insGTTTAGGTACAAAAA MANE Select	ENSP00000286548.4:n.606-81_606-80insGTTTAGGTACAAAAA
ENST00000286548.8:c.606-81_606-80insGTTTAGGTACAAAAA	ENSP00000286548.4:n.606-81_606-80insGTTTAGGTACAAAAA
NM_002072.4:c.606-81_606-80insGTTTAGGTACAAAAA	NP_002063.2:n.606-81_606-80insGTTTAGGTACAAAAA
XM_017014628.2:c.432-81_432-80insGTTTAGGTACAAAAA	XP_016870117.1:n.432-81_432-80insGTTTAGGTACAAAAA
NM_002072.5:c.606-81_606-80insGTTTAGGTACAAAAA MANE Select	NP_002063.2:n.606-81_606-80insGTTTAGGTACAAAAA