Canonical Allele Identifier: CA1201830789

Gene: FCER1A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159302368G= , CM000663.2:g.159302368G=	GRCh38
NC_000001.10:g.159272158G= , CM000663.1:g.159272158G=	GRCh37
NC_000001.9:g.157538782G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000693622.1:c.4G= MANE Select	ENSP00000509626.1:p.Ala2=
ENST00000368114.1:c.4G=	ENSP00000357096.1:p.Ala2=
ENST00000368115.5:c.4G=	ENSP00000357097.1:p.Ala2=
NM_002001.3:c.4G=	NP_001992.1:p.Ala2=
NM_001387280.1:c.4G= MANE Select	NP_001374209.1:p.Ala2=
NM_001387281.1:c.4G=	NP_001374210.1:p.Ala2=
NM_001387282.1:c.4G=	NP_001374211.1:p.Ala2=
NM_002001.4:c.4G=	NP_001992.1:p.Ala2=