Canonical Allele Identifier: CA548332104

Gene: GNB4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179405426del , CM000665.2:g.179405426del	GRCh38
NC_000003.11:g.179123214del , CM000665.1:g.179123214del	GRCh37
NC_000003.10:g.180605908del	NCBI36
NG_033163.1:g.51160del

Transcript Alleles

HGVS	Amino-acid Change
NM_021629.4:c.700-18del MANE Select	NP_067642.1:n.700-18del
ENST00000232564.8:c.700-18del MANE Select	ENSP00000232564.3:n.700-18del
NM_021629.3:c.700-18del	NP_067642.1:n.700-18del
ENST00000232564.7:c.700-18del	ENSP00000232564.3:n.700-18del
ENST00000466899.5:c.467-4105del
ENST00000466899.6:c.700-4105del	ENSP00000420066.2:n.700-4105del
ENST00000468623.5:c.700-18del	ENSP00000419693.1:n.700-18del
ENST00000468623.6:c.661-18del	ENSP00000419693.2:n.661-18del
ENST00000674713.1:c.592-18del	ENSP00000502144.1:n.592-18del
ENST00000674862.1:c.700-18del	ENSP00000502628.1:n.700-18del
ENST00000674927.1:c.700-18del	ENSP00000501774.1:n.700-18del
ENST00000675901.1:c.700-18del	ENSP00000501992.1:n.700-18del
ENST00000676128.1:c.700-18del	ENSP00000501882.1:n.700-18del
XM_005247692.1:c.700-18del	XP_005247749.1:n.700-18del
XM_005247692.2:c.700-18del	XP_005247749.1:n.700-18del
XM_006713721.1:c.700-18del	XP_006713784.1:n.700-18del
XM_006713721.2:c.700-18del	XP_006713784.1:n.700-18del