Canonical Allele Identifier: CA2321045691

Gene: FCER2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7689923_7689924delinsAC , CM000681.2:g.7689923_7689924delinsAC	GRCh38
NC_000019.9:g.7754809_7754810delinsAC , CM000681.1:g.7754809_7754810delinsAC	GRCh37
NC_000019.8:g.7660809_7660810delinsAC	NCBI36
NG_029554.1:g.17223_17224delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.728+235_728+236delinsGT MANE Select	ENSP00000471974.1:n.728+235_728+236delinsGT
ENST00000346664.9:c.728+235_728+236delinsGT	ENSP00000264072.6:n.728+235_728+236delinsGT
ENST00000360067.8:c.725+235_725+236delinsGT	ENSP00000353178.4:n.725+235_725+236delinsGT
ENST00000597312.5:n.1253+235_1253+236delinsGT
ENST00000597921.5:c.728+235_728+236delinsGT	ENSP00000471974.1:n.728+235_728+236delinsGT
ENST00000597934.1:n.1090+235_1090+236delinsGT
ENST00000598803.5:n.1223+235_1223+236delinsGT
NM_001207019.2:c.725+235_725+236delinsGT	NP_001193948.2:n.725+235_725+236delinsGT
NM_001220500.1:c.728+235_728+236delinsGT	NP_001207429.1:n.728+235_728+236delinsGT
NM_002002.4:c.728+235_728+236delinsGT	NP_001993.2:n.728+235_728+236delinsGT
XM_005272462.3:c.728+235_728+236delinsGT	XP_005272519.1:n.728+235_728+236delinsGT
XM_005272462.4:c.728+235_728+236delinsGT	XP_005272519.1:n.728+235_728+236delinsGT
NM_001220500.2:c.728+235_728+236delinsGT MANE Select	NP_001207429.1:n.728+235_728+236delinsGT
NM_001207019.3:c.725+235_725+236delinsGT	NP_001193948.2:n.725+235_725+236delinsGT
NM_002002.5:c.728+235_728+236delinsGT	NP_001993.2:n.728+235_728+236delinsGT