Canonical Allele Identifier: CA1201830797

Gene: FCER1A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159302391T= , CM000663.2:g.159302391T=	GRCh38
NC_000001.10:g.159272181T= , CM000663.1:g.159272181T=	GRCh37
NC_000001.9:g.157538805T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000693622.1:c.27T= MANE Select	ENSP00000509626.1:p.Thr9=
ENST00000368114.1:c.27T=	ENSP00000357096.1:p.Thr9=
ENST00000368115.5:c.27T=	ENSP00000357097.1:p.Thr9=
NM_002001.3:c.27T=	NP_001992.1:p.Thr9=
NM_001387280.1:c.27T= MANE Select	NP_001374209.1:p.Thr9=
NM_001387281.1:c.27T=	NP_001374210.1:p.Thr9=
NM_001387282.1:c.27T=	NP_001374211.1:p.Thr9=
NM_002001.4:c.27T=	NP_001992.1:p.Thr9=