Canonical Allele Identifier: CA1857429496

Gene: GNAQ

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.77794623_77794625delinsCAT , CM000671.2:g.77794623_77794625delinsCAT	GRCh38
NC_000009.11:g.80409539_80409541delinsCAT , CM000671.1:g.80409539_80409541delinsCAT	GRCh37
NC_000009.10:g.79599359_79599361delinsCAT	NCBI36
NG_027904.2:g.241679_241681delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286548.9:c.606-33_606-31delinsATG MANE Select	ENSP00000286548.4:n.606-33_606-31delinsATG
ENST00000286548.8:c.606-33_606-31delinsATG	ENSP00000286548.4:n.606-33_606-31delinsATG
NM_002072.4:c.606-33_606-31delinsATG	NP_002063.2:n.606-33_606-31delinsATG
XM_017014628.2:c.432-33_432-31delinsATG	XP_016870117.1:n.432-33_432-31delinsATG
NM_002072.5:c.606-33_606-31delinsATG MANE Select	NP_002063.2:n.606-33_606-31delinsATG