Canonical Allele Identifier: CA1201831484
Gene: FCER1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159304005A= , CM000663.2:g.159304005A= GRCh38
NC_000001.10:g.159273795A= , CM000663.1:g.159273795A= GRCh37
NC_000001.9:g.157540419A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000693622.1:c.154A= MANE Select ENSP00000509626.1:p.Asn52=
ENST00000368114.1:c.77-22A= ENSP00000357096.1:n.77-22A=
ENST00000368115.5:c.154A= ENSP00000357097.1:p.Asn52=
NM_002001.3:c.154A= NP_001992.1:p.Asn52=
NM_001387280.1:c.154A= MANE Select NP_001374209.1:p.Asn52=
NM_001387281.1:c.76+1131A= NP_001374210.1:n.76+1131A=
NM_001387282.1:c.77-22A= NP_001374211.1:n.77-22A=
NM_002001.4:c.154A= NP_001992.1:p.Asn52=