Canonical Allele Identifier: CA2321045907

Gene: FCER2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690355_7690356delinsTC , CM000681.2:g.7690355_7690356delinsTC	GRCh38
NC_000019.9:g.7755241_7755242delinsTC , CM000681.1:g.7755241_7755242delinsTC	GRCh37
NC_000019.8:g.7661241_7661242delinsTC	NCBI36
NG_029554.1:g.16791_16792delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.621+50_621+51delinsGA MANE Select	ENSP00000471974.1:n.621+50_621+51delinsGA
ENST00000346664.9:c.621+50_621+51delinsGA	ENSP00000264072.6:n.621+50_621+51delinsGA
ENST00000360067.8:c.618+50_618+51delinsGA	ENSP00000353178.4:n.618+50_618+51delinsGA
ENST00000597312.5:n.1146+50_1146+51delinsGA
ENST00000597921.5:c.621+50_621+51delinsGA	ENSP00000471974.1:n.621+50_621+51delinsGA
ENST00000597934.1:n.983+50_983+51delinsGA
ENST00000598803.5:n.1116+50_1116+51delinsGA
NM_001207019.2:c.618+50_618+51delinsGA	NP_001193948.2:n.618+50_618+51delinsGA
NM_001220500.1:c.621+50_621+51delinsGA	NP_001207429.1:n.621+50_621+51delinsGA
NM_002002.4:c.621+50_621+51delinsGA	NP_001993.2:n.621+50_621+51delinsGA
XM_005272462.3:c.621+50_621+51delinsGA	XP_005272519.1:n.621+50_621+51delinsGA
XM_005272462.4:c.621+50_621+51delinsGA	XP_005272519.1:n.621+50_621+51delinsGA
NM_001220500.2:c.621+50_621+51delinsGA MANE Select	NP_001207429.1:n.621+50_621+51delinsGA
NM_001207019.3:c.618+50_618+51delinsGA	NP_001193948.2:n.618+50_618+51delinsGA
NM_002002.5:c.621+50_621+51delinsGA	NP_001993.2:n.621+50_621+51delinsGA