Canonical Allele Identifier: CA343059237
Gene: FCER1A HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000693622.1:c.260A>C MANE Select ENSP00000509626.1:p.Asp87Ala
ENST00000368114.1:c.161A>C ENSP00000357096.1:p.Asp54Ala
ENST00000368115.5:c.260A>C ENSP00000357097.1:p.Asp87Ala
NM_002001.3:c.260A>C NP_001992.1:p.Asp87Ala
NM_001387280.1:c.260A>C MANE Select NP_001374209.1:p.Asp87Ala
NM_001387281.1:c.76+1237A>C NP_001374210.1:n.76+1237A>C
NM_001387282.1:c.161A>C NP_001374211.1:p.Asp54Ala
NM_002001.4:c.260A>C NP_001992.1:p.Asp87Ala