Canonical Allele Identifier: CA2552109788

Gene: GNAQ

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.77794161del , CM000671.2:g.77794161del	GRCh38
NC_000009.11:g.80409077del , CM000671.1:g.80409077del	GRCh37
NC_000009.10:g.79598897del	NCBI36
NG_027904.2:g.242144del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286548.9:c.735+303del MANE Select	ENSP00000286548.4:n.735+303del
ENST00000286548.8:c.735+303del	ENSP00000286548.4:n.735+303del
NM_002072.4:c.735+303del	NP_002063.2:n.735+303del
XM_017014628.2:c.561+303del	XP_016870117.1:n.561+303del
NM_002072.5:c.735+303del MANE Select	NP_002063.2:n.735+303del