Canonical Allele Identifier: CA2690385158
Gene: GNAQ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794579dup , CM000671.2:g.77794579dup GRCh38
NC_000009.11:g.80409495dup , CM000671.1:g.80409495dup GRCh37
NC_000009.10:g.79599315dup NCBI36
NG_027904.2:g.241729dup

Transcript Alleles

HGVS Amino-acid change
ENST00000286548.9:c.623dup MANE Select ENSP00000286548.4:p.Gln209ProfsTer13
ENST00000286548.8:c.623dup ENSP00000286548.4:p.Gln209ProfsTer13
NM_002072.4:c.623dup NP_002063.2:p.Gln209ProfsTer13
XM_017014628.2:c.449dup XP_016870117.1:p.Gln151ProfsTer13
NM_002072.5:c.623dup MANE Select NP_002063.2:p.Gln209ProfsTer13