Canonical Allele Identifier: CA2690385141

Gene: GNAQ

Linked Data

• gnomAD v4: 9-77794448-CTAAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.77794449_77794452del , CM000671.2:g.77794449_77794452del	GRCh38
NC_000009.11:g.80409365_80409368del , CM000671.1:g.80409365_80409368del	GRCh37
NC_000009.10:g.79599185_79599188del	NCBI36
NG_027904.2:g.241852_241855del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286548.9:c.735+11_735+14del MANE Select	ENSP00000286548.4:n.735+11_735+14del
ENST00000286548.8:c.735+11_735+14del	ENSP00000286548.4:n.735+11_735+14del
NM_002072.4:c.735+11_735+14del	NP_002063.2:n.735+11_735+14del
XM_017014628.2:c.561+11_561+14del	XP_016870117.1:n.561+11_561+14del
NM_002072.5:c.735+11_735+14del MANE Select	NP_002063.2:n.735+11_735+14del