Canonical Allele Identifier: CA2690385143

Gene: GNAQ

Linked Data

• gnomAD v4: 9-77794449-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.77794452del , CM000671.2:g.77794452del	GRCh38
NC_000009.11:g.80409368del , CM000671.1:g.80409368del	GRCh37
NC_000009.10:g.79599188del	NCBI36
NG_027904.2:g.241854del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286548.9:c.735+13del MANE Select	ENSP00000286548.4:n.735+13del
ENST00000286548.8:c.735+13del	ENSP00000286548.4:n.735+13del
NM_002072.4:c.735+13del	NP_002063.2:n.735+13del
XM_017014628.2:c.561+13del	XP_016870117.1:n.561+13del
NM_002072.5:c.735+13del MANE Select	NP_002063.2:n.735+13del