Canonical Allele Identifier: CA1857429443
Gene: GNAQ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794572_77794573delinsTG , CM000671.2:g.77794572_77794573delinsTG GRCh38
NC_000009.11:g.80409488_80409489delinsTG , CM000671.1:g.80409488_80409489delinsTG GRCh37
NC_000009.10:g.79599308_79599309delinsTG NCBI36
NG_027904.2:g.241731_241732delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000286548.9:c.625_626delinsCA MANE Select ENSP00000286548.4:p.Gln209=
ENST00000286548.8:c.625_626delinsCA ENSP00000286548.4:p.Gln209=
NM_002072.4:c.625_626delinsCA NP_002063.2:p.Gln209=
XM_017014628.2:c.451_452delinsCA XP_016870117.1:p.Gln151=
NM_002072.5:c.625_626delinsCA MANE Select NP_002063.2:p.Gln209=