Canonical Allele Identifier: CA2712366

Gene: GNB4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179401331dup , CM000665.2:g.179401331dup	GRCh38
NC_000003.11:g.179119119dup , CM000665.1:g.179119119dup	GRCh37
NC_000003.10:g.180601813dup	NCBI36
NG_033163.1:g.55261dup

Transcript Alleles

HGVS	Amino-acid Change
NM_021629.4:c.917-4dup MANE Select	NP_067642.1:n.917-4dup
ENST00000232564.8:c.917-4dup MANE Select	ENSP00000232564.3:n.917-4dup
NM_021629.3:c.917-4dup	NP_067642.1:n.917-4dup
ENST00000232564.7:c.917-4dup	ENSP00000232564.3:n.917-4dup
ENST00000466899.5:c.467-4dup
ENST00000466899.6:c.700-4dup	ENSP00000420066.2:n.700-4dup
ENST00000468623.5:c.917-4dup	ENSP00000419693.1:n.917-4dup
ENST00000468623.6:c.878-4dup	ENSP00000419693.2:n.878-4dup
ENST00000674713.1:c.809-4dup	ENSP00000502144.1:n.809-4dup
ENST00000674862.1:c.917-4dup	ENSP00000502628.1:n.917-4dup
ENST00000676128.1:c.917-4dup	ENSP00000501882.1:n.917-4dup
XM_005247692.1:c.917-4dup	XP_005247749.1:n.917-4dup
XM_005247692.2:c.917-4dup	XP_005247749.1:n.917-4dup
XM_006713721.1:c.917-4dup	XP_006713784.1:n.917-4dup
XM_006713721.2:c.917-4dup	XP_006713784.1:n.917-4dup