Canonical Allele Identifier: CA2576600331

Gene: FCER2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690538_7690547del , CM000681.2:g.7690538_7690547del	GRCh38
NC_000019.9:g.7755424_7755433del , CM000681.1:g.7755424_7755433del	GRCh37
NC_000019.8:g.7661424_7661433del	NCBI36
NG_029554.1:g.16601_16610del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.481_490del MANE Select	ENSP00000471974.1:p.Asn161LeufsTer?
ENST00000346664.9:c.481_490del	ENSP00000264072.6:p.Asn161LeufsTer?
ENST00000360067.8:c.478_487del	ENSP00000353178.4:p.Asn160LeufsTer?
ENST00000593418.1:c.418_427del	ENSP00000472067.1:p.Asn140LeufsTer?
ENST00000597312.5:n.1006_1015del
ENST00000597921.5:c.481_490del	ENSP00000471974.1:p.Asn161LeufsTer?
ENST00000597934.1:n.843_852del
ENST00000598803.5:n.976_985del
NM_001207019.2:c.478_487del	NP_001193948.2:p.Asn160LeufsTer?
NM_001220500.1:c.481_490del	NP_001207429.1:p.Asn161LeufsTer?
NM_002002.4:c.481_490del	NP_001993.2:p.Asn161LeufsTer?
XM_005272462.3:c.481_490del	XP_005272519.1:p.Asn161LeufsTer?
XM_005272462.4:c.481_490del	XP_005272519.1:p.Asn161LeufsTer?
NM_001220500.2:c.481_490del MANE Select	NP_001207429.1:p.Asn161LeufsTer?
NM_001207019.3:c.478_487del	NP_001193948.2:p.Asn160LeufsTer?
NM_002002.5:c.481_490del	NP_001993.2:p.Asn161LeufsTer?