Canonical Allele Identifier: CA2677392572
Gene: CD83 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.14133872_14133874del , CM000668.2:g.14133872_14133874del GRCh38
NC_000006.11:g.14134103_14134105del , CM000668.1:g.14134103_14134105del GRCh37
NC_000006.10:g.14242082_14242084del NCBI36
NG_030372.1:g.21617_21619del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379153.4:c.489+117_489+119del MANE Select ENSP00000368450.3:n.489+117_489+119del
ENST00000379153.3:c.489+117_489+119del ENSP00000368450.3:n.489+117_489+119del
ENST00000612003.4:c.312+117_312+119del ENSP00000480760.1:n.312+117_312+119del
NM_001040280.1:c.489+117_489+119del NP_001035370.1:n.489+117_489+119del
NM_001251901.1:c.312+117_312+119del NP_001238830.1:n.312+117_312+119del
NM_004233.3:c.489+117_489+119del NP_004224.1:n.489+117_489+119del
NM_004233.4:c.489+117_489+119del MANE Select NP_004224.1:n.489+117_489+119del
NM_001040280.2:c.489+117_489+119del NP_001035370.1:n.489+117_489+119del
NM_001040280.3:c.489+117_489+119del NP_001035370.1:n.489+117_489+119del