Canonical Allele Identifier: CA2648764909
Gene: FCER1G HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161219068del , CM000663.2:g.161219068del GRCh38
NC_000001.10:g.161188858del , CM000663.1:g.161188858del GRCh37
NC_000001.9:g.159455482del NCBI36
NG_029043.1:g.8772del

Transcript Alleles

HGVS Amino-acid Change
ENST00000289902.2:c.*125del MANE Select ENSP00000289902.1:n.*125del
ENST00000289902.1:c.*125del ENSP00000289902.1:n.*125del
ENST00000367992.7:c.198+345del ENSP00000356971.3:n.198+345del
ENST00000490414.1:n.382del
NM_004106.1:c.*125del NP_004097.1:n.*125del
NM_004106.2:c.*125del MANE Select NP_004097.1:n.*125del