Canonical Allele Identifier: CA2668635329
Gene: GNB4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179420797_179420801del , CM000665.2:g.179420797_179420801del GRCh38
NC_000003.11:g.179138585_179138589del , CM000665.1:g.179138585_179138589del GRCh37
NC_000003.10:g.180621279_180621283del NCBI36
NG_033163.1:g.35783_35787del

Transcript Alleles

HGVS Amino-acid change
ENST00000232564.8:c.96+88_96+92del MANE Select ENSP00000232564.3:n.96+88_96+92del
ENST00000465153.2:c.96+88_96+92del ENSP00000502010.1:n.96+88_96+92del
ENST00000466899.6:c.96+88_96+92del ENSP00000420066.2:n.96+88_96+92del
ENST00000468623.6:c.58-1296_58-1292del ENSP00000419693.2:n.58-1296_58-1292del
ENST00000674713.1:c.-13+88_-13+92del ENSP00000502144.1:n.-13+88_-13+92del
ENST00000674862.1:c.96+88_96+92del ENSP00000502628.1:n.96+88_96+92del
ENST00000674927.1:c.96+88_96+92del ENSP00000501774.1:n.96+88_96+92del
ENST00000675901.1:c.96+88_96+92del ENSP00000501992.1:n.96+88_96+92del
ENST00000676128.1:c.96+88_96+92del ENSP00000501882.1:n.96+88_96+92del
ENST00000232564.7:c.96+88_96+92del ENSP00000232564.3:n.96+88_96+92del
ENST00000468623.5:c.96+88_96+92del ENSP00000419693.1:n.96+88_96+92del
ENST00000497513.1:c.96+88_96+92del ENSP00000420606.1:n.96+88_96+92del
NM_021629.3:c.96+88_96+92del NP_067642.1:n.96+88_96+92del
XM_005247692.1:c.96+88_96+92del XP_005247749.1:n.96+88_96+92del
XM_006713721.1:c.96+88_96+92del XP_006713784.1:n.96+88_96+92del
XM_011513061.1:c.96+88_96+92del XP_011511363.1:n.96+88_96+92del
XM_005247692.2:c.96+88_96+92del XP_005247749.1:n.96+88_96+92del
XM_006713721.2:c.96+88_96+92del XP_006713784.1:n.96+88_96+92del
NM_021629.4:c.96+88_96+92del MANE Select NP_067642.1:n.96+88_96+92del