Canonical Allele Identifier: CA645561181
Gene: GNAQ HGNC NCBI

Linked Data

dbSNP Id: rs2118444329
COSMIC: COSM28761

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794571_77794573delinsATA , CM000671.2:g.77794571_77794573delinsATA GRCh38
NC_000009.11:g.80409487_80409489delinsATA , CM000671.1:g.80409487_80409489delinsATA GRCh37
NC_000009.10:g.79599307_79599309delinsATA NCBI36
NG_027904.2:g.241731_241733delinsTAT

Transcript Alleles

HGVS Amino-acid change
ENST00000286548.9:c.625_627delinsTAT MANE Select ENSP00000286548.4:p.Gln209Tyr
ENST00000286548.8:c.625_627delinsTAT ENSP00000286548.4:p.Gln209Tyr
NM_002072.4:c.625_627delinsTAT NP_002063.2:p.Gln209Tyr
XM_017014628.2:c.451_453delinsTAT XP_016870117.1:p.Gln151Tyr
NM_002072.5:c.625_627delinsTAT MANE Select NP_002063.2:p.Gln209Tyr