Canonical Allele Identifier: CA1857429264

Gene: GNAQ

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.77794396_77794400delinsACTTT , CM000671.2:g.77794396_77794400delinsACTTT	GRCh38
NC_000009.11:g.80409312_80409316delinsACTTT , CM000671.1:g.80409312_80409316delinsACTTT	GRCh37
NC_000009.10:g.79599132_79599136delinsACTTT	NCBI36
NG_027904.2:g.241904_241908delinsAAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286548.9:c.735+63_735+67delinsAAAGT MANE Select	ENSP00000286548.4:n.735+63_735+67delinsAAAGT
ENST00000286548.8:c.735+63_735+67delinsAAAGT	ENSP00000286548.4:n.735+63_735+67delinsAAAGT
NM_002072.4:c.735+63_735+67delinsAAAGT	NP_002063.2:n.735+63_735+67delinsAAAGT
XM_017014628.2:c.561+63_561+67delinsAAAGT	XP_016870117.1:n.561+63_561+67delinsAAAGT
NM_002072.5:c.735+63_735+67delinsAAAGT MANE Select	NP_002063.2:n.735+63_735+67delinsAAAGT