Canonical Allele Identifier: CA2576600318

Gene: FCER2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690205_7690210del , CM000681.2:g.7690205_7690210del	GRCh38
NC_000019.9:g.7755091_7755096del , CM000681.1:g.7755091_7755096del	GRCh37
NC_000019.8:g.7661091_7661096del	NCBI36
NG_029554.1:g.16939_16944del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.679_684del MANE Select	ENSP00000471974.1:p.Asp227_Leu228del
ENST00000346664.9:c.679_684del	ENSP00000264072.6:p.Asp227_Leu228del
ENST00000360067.8:c.676_681del	ENSP00000353178.4:p.Asp226_Leu227del
ENST00000597312.5:n.1204_1209del
ENST00000597921.5:c.679_684del	ENSP00000471974.1:p.Asp227_Leu228del
ENST00000597934.1:n.1041_1046del
ENST00000598803.5:n.1174_1179del
NM_001207019.2:c.676_681del	NP_001193948.2:p.Asp226_Leu227del
NM_001220500.1:c.679_684del	NP_001207429.1:p.Asp227_Leu228del
NM_002002.4:c.679_684del	NP_001993.2:p.Asp227_Leu228del
XM_005272462.3:c.679_684del	XP_005272519.1:p.Asp227_Leu228del
XM_005272462.4:c.679_684del	XP_005272519.1:p.Asp227_Leu228del
NM_001220500.2:c.679_684del MANE Select	NP_001207429.1:p.Asp227_Leu228del
NM_001207019.3:c.676_681del	NP_001193948.2:p.Asp226_Leu227del
NM_002002.5:c.679_684del	NP_001993.2:p.Asp227_Leu228del