Canonical Allele Identifier: CA1141846466
Gene: FCER1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159302379G= , CM000663.2:g.159302379G= GRCh38
NC_000001.10:g.159272169G= , CM000663.1:g.159272169G= GRCh37
NC_000001.9:g.157538793G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000693622.1:c.15G= MANE Select ENSP00000509626.1:p.Met5=
ENST00000368114.1:c.15G= ENSP00000357096.1:p.Met5=
ENST00000368115.5:c.15G= ENSP00000357097.1:p.Met5=
NM_002001.3:c.15G= NP_001992.1:p.Met5=
NM_001387280.1:c.15G= MANE Select NP_001374209.1:p.Met5=
NM_001387281.1:c.15G= NP_001374210.1:p.Met5=
NM_001387282.1:c.15G= NP_001374211.1:p.Met5=
NM_002001.4:c.15G= NP_001992.1:p.Met5=