Canonical Allele Identifier: CA1202650823
Gene: FCER1G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161219050_161219051delinsCT , CM000663.2:g.161219050_161219051delinsCT GRCh38
NC_000001.10:g.161188840_161188841delinsCT , CM000663.1:g.161188840_161188841delinsCT GRCh37
NC_000001.9:g.159455464_159455465delinsCT NCBI36
NG_029043.1:g.8754_8755delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000289902.2:c.*107_*108delinsCT MANE Select ENSP00000289902.1:n.*107_*108delinsCT
ENST00000289902.1:c.*107_*108delinsCT ENSP00000289902.1:n.*107_*108delinsCT
ENST00000367992.7:c.198+327_198+328delinsCT ENSP00000356971.3:n.198+327_198+328delinsCT
ENST00000490414.1:n.364_365delinsCT
NM_004106.1:c.*107_*108delinsCT NP_004097.1:n.*107_*108delinsCT
NM_004106.2:c.*107_*108delinsCT MANE Select NP_004097.1:n.*107_*108delinsCT