Canonical Allele Identifier: CA1201831519
Gene: FCER1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159304106T= , CM000663.2:g.159304106T= GRCh38
NC_000001.10:g.159273896T= , CM000663.1:g.159273896T= GRCh37
NC_000001.9:g.157540520T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000693622.1:c.255T= MANE Select ENSP00000509626.1:p.Phe85=
ENST00000368114.1:c.156T= ENSP00000357096.1:p.Phe52=
ENST00000368115.5:c.255T= ENSP00000357097.1:p.Phe85=
NM_002001.3:c.255T= NP_001992.1:p.Phe85=
NM_001387280.1:c.255T= MANE Select NP_001374209.1:p.Phe85=
NM_001387281.1:c.76+1232T= NP_001374210.1:n.76+1232T=
NM_001387282.1:c.156T= NP_001374211.1:p.Phe52=
NM_002001.4:c.255T= NP_001992.1:p.Phe85=