Canonical Allele Identifier: CA1201831521
Gene: FCER1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159304111A= , CM000663.2:g.159304111A= GRCh38
NC_000001.10:g.159273901A= , CM000663.1:g.159273901A= GRCh37
NC_000001.9:g.157540525A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000693622.1:c.260A= MANE Select ENSP00000509626.1:p.Asp87=
ENST00000368114.1:c.161A= ENSP00000357096.1:p.Asp54=
ENST00000368115.5:c.260A= ENSP00000357097.1:p.Asp87=
NM_002001.3:c.260A= NP_001992.1:p.Asp87=
NM_001387280.1:c.260A= MANE Select NP_001374209.1:p.Asp87=
NM_001387281.1:c.76+1237A= NP_001374210.1:n.76+1237A=
NM_001387282.1:c.161A= NP_001374211.1:p.Asp54=
NM_002001.4:c.260A= NP_001992.1:p.Asp87=