Canonical Allele Identifier: CA2321046003

Gene: FCER2

Linked Data

• dbSNP Id: rs777127227

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690536_7690540dup , CM000681.2:g.7690536_7690540dup	GRCh38
NC_000019.9:g.7755422_7755426dup , CM000681.1:g.7755422_7755426dup	GRCh37
NC_000019.8:g.7661422_7661426dup	NCBI36
NG_029554.1:g.16609_16613dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.489_493dup MANE Select	ENSP00000471974.1:p.Glu165AlafsTer?
ENST00000346664.9:c.489_493dup	ENSP00000264072.6:p.Glu165AlafsTer?
ENST00000360067.8:c.486_490dup	ENSP00000353178.4:p.Glu164AlafsTer?
ENST00000593418.1:c.426_430dup	ENSP00000472067.1:p.Glu144AlafsTer?
ENST00000597312.5:n.1014_1018dup
ENST00000597921.5:c.489_493dup	ENSP00000471974.1:p.Glu165AlafsTer?
ENST00000597934.1:n.851_855dup
ENST00000598803.5:n.984_988dup
NM_001207019.2:c.486_490dup	NP_001193948.2:p.Glu164AlafsTer?
NM_001220500.1:c.489_493dup	NP_001207429.1:p.Glu165AlafsTer?
NM_002002.4:c.489_493dup	NP_001993.2:p.Glu165AlafsTer?
XM_005272462.3:c.489_493dup	XP_005272519.1:p.Glu165AlafsTer?
XM_005272462.4:c.489_493dup	XP_005272519.1:p.Glu165AlafsTer?
NM_001220500.2:c.489_493dup MANE Select	NP_001207429.1:p.Glu165AlafsTer?
NM_001207019.3:c.486_490dup	NP_001193948.2:p.Glu164AlafsTer?
NM_002002.5:c.489_493dup	NP_001993.2:p.Glu165AlafsTer?