Canonical Allele Identifier: CA2690384996
Gene: GNAQ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794314dup , CM000671.2:g.77794314dup GRCh38
NC_000009.11:g.80409230dup , CM000671.1:g.80409230dup GRCh37
NC_000009.10:g.79599050dup NCBI36
NG_027904.2:g.241991dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000286548.9:c.735+150dup MANE Select ENSP00000286548.4:n.735+150dup
ENST00000286548.8:c.735+150dup ENSP00000286548.4:n.735+150dup
NM_002072.4:c.735+150dup NP_002063.2:n.735+150dup
XM_017014628.2:c.561+150dup XP_016870117.1:n.561+150dup
NM_002072.5:c.735+150dup MANE Select NP_002063.2:n.735+150dup