Canonical Allele Identifier: CA2321046047

Gene: FCER2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690595_7690597delinsAAG , CM000681.2:g.7690595_7690597delinsAAG	GRCh38
NC_000019.9:g.7755481_7755483delinsAAG , CM000681.1:g.7755481_7755483delinsAAG	GRCh37
NC_000019.8:g.7661481_7661483delinsAAG	NCBI36
NG_029554.1:g.16550_16552delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.470-40_470-38delinsCTT MANE Select	ENSP00000471974.1:n.470-40_470-38delinsCTT
ENST00000346664.9:c.470-40_470-38delinsCTT	ENSP00000264072.6:n.470-40_470-38delinsCTT
ENST00000360067.8:c.467-40_467-38delinsCTT	ENSP00000353178.4:n.467-40_467-38delinsCTT
ENST00000593418.1:c.407-40_407-38delinsCTT	ENSP00000472067.1:n.407-40_407-38delinsCTT
ENST00000597312.5:n.995-40_995-38delinsCTT
ENST00000597921.5:c.470-40_470-38delinsCTT	ENSP00000471974.1:n.470-40_470-38delinsCTT
ENST00000597934.1:n.832-40_832-38delinsCTT
ENST00000598803.5:n.965-40_965-38delinsCTT
NM_001207019.2:c.467-40_467-38delinsCTT	NP_001193948.2:n.467-40_467-38delinsCTT
NM_001220500.1:c.470-40_470-38delinsCTT	NP_001207429.1:n.470-40_470-38delinsCTT
NM_002002.4:c.470-40_470-38delinsCTT	NP_001993.2:n.470-40_470-38delinsCTT
XM_005272462.3:c.470-40_470-38delinsCTT	XP_005272519.1:n.470-40_470-38delinsCTT
XM_005272462.4:c.470-40_470-38delinsCTT	XP_005272519.1:n.470-40_470-38delinsCTT
NM_001220500.2:c.470-40_470-38delinsCTT MANE Select	NP_001207429.1:n.470-40_470-38delinsCTT
NM_001207019.3:c.467-40_467-38delinsCTT	NP_001193948.2:n.467-40_467-38delinsCTT
NM_002002.5:c.470-40_470-38delinsCTT	NP_001993.2:n.470-40_470-38delinsCTT