Canonical Allele Identifier: CA2813484168

Gene: FCER2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690343_7690344insAAGGCCCCGGGCACATGTCTCCAGTCCTCGGGGCCTTCCAGCCCACTTTGAGAGGT , CM000681.2:g.7690343_7690344insAAGGCCCCGGGCACATGTCTCCAGTCCTCGGGGCCTTCCAGCCCACTTTGAGAGGT	GRCh38
NC_000019.9:g.7755229_7755230insAAGGCCCCGGGCACATGTCTCCAGTCCTCGGGGCCTTCCAGCCCACTTTGAGAGGT , CM000681.1:g.7755229_7755230insAAGGCCCCGGGCACATGTCTCCAGTCCTCGGGGCCTTCCAGCCCACTTTGAGAGGT	GRCh37
NC_000019.8:g.7661229_7661230insAAGGCCCCGGGCACATGTCTCCAGTCCTCGGGGCCTTCCAGCCCACTTTGAGAGGT	NCBI36
NG_029554.1:g.16803_16804insACCTCTCAAAGTGGGCTGGAAGGCCCCGAGGACTGGAGACATGTGCCCGGGGCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.621+62_621+63insACCTCTCAAAGTGGGCTGGAAGGCCCCGAGGACTGGAGACATGTGCCCGGGGCCTT MANE Select	ENSP00000471974.1:n.621+62_621+63insACCTCTCAAAGTGGGCTGGAAGGCC...
ENST00000346664.9:c.621+62_621+63insACCTCTCAAAGTGGGCTGGAAGGCCCCGAGGACTGGAGACATGTGCCCGGGGCCTT	ENSP00000264072.6:n.621+62_621+63insACCTCTCAAAGTGGGCTGGAAGGCC...
ENST00000360067.8:c.618+62_618+63insACCTCTCAAAGTGGGCTGGAAGGCCCCGAGGACTGGAGACATGTGCCCGGGGCCTT	ENSP00000353178.4:n.618+62_618+63insACCTCTCAAAGTGGGCTGGAAGGCC...
ENST00000597312.5:n.1146+62_1146+63insACCTCTCAAAGTGGGCTGGAAGGCCCCGAGGACTGGAGACATGTGCCCGGGGCCTT
ENST00000597921.5:c.621+62_621+63insACCTCTCAAAGTGGGCTGGAAGGCCCCGAGGACTGGAGACATGTGCCCGGGGCCTT	ENSP00000471974.1:n.621+62_621+63insACCTCTCAAAGTGGGCTGGAAGGCC...
ENST00000597934.1:n.983+62_983+63insACCTCTCAAAGTGGGCTGGAAGGCCCCGAGGACTGGAGACATGTGCCCGGGGCCTT
ENST00000598803.5:n.1116+62_1116+63insACCTCTCAAAGTGGGCTGGAAGGCCCCGAGGACTGGAGACATGTGCCCGGGGCCTT
NM_001207019.2:c.618+62_618+63insACCTCTCAAAGTGGGCTGGAAGGCCCCGAGGACTGGAGACATGTGCCCGGGGCCTT	NP_001193948.2:n.618+62_618+63insACCTCTCAAAGTGGGCTGGAAGGCCCCG...
NM_001220500.1:c.621+62_621+63insACCTCTCAAAGTGGGCTGGAAGGCCCCGAGGACTGGAGACATGTGCCCGGGGCCTT	NP_001207429.1:n.621+62_621+63insACCTCTCAAAGTGGGCTGGAAGGCCCCG...
NM_002002.4:c.621+62_621+63insACCTCTCAAAGTGGGCTGGAAGGCCCCGAGGACTGGAGACATGTGCCCGGGGCCTT	NP_001993.2:n.621+62_621+63insACCTCTCAAAGTGGGCTGGAAGGCCCCGAGG...
XM_005272462.3:c.621+62_621+63insACCTCTCAAAGTGGGCTGGAAGGCCCCGAGGACTGGAGACATGTGCCCGGGGCCTT	XP_005272519.1:n.621+62_621+63insACCTCTCAAAGTGGGCTGGAAGGCCCCG...
XM_005272462.4:c.621+62_621+63insACCTCTCAAAGTGGGCTGGAAGGCCCCGAGGACTGGAGACATGTGCCCGGGGCCTT	XP_005272519.1:n.621+62_621+63insACCTCTCAAAGTGGGCTGGAAGGCCCCG...
NM_001220500.2:c.621+62_621+63insACCTCTCAAAGTGGGCTGGAAGGCCCCGAGGACTGGAGACATGTGCCCGGGGCCTT MANE Select	NP_001207429.1:n.621+62_621+63insACCTCTCAAAGTGGGCTGGAAGGCCCCG...
NM_001207019.3:c.618+62_618+63insACCTCTCAAAGTGGGCTGGAAGGCCCCGAGGACTGGAGACATGTGCCCGGGGCCTT	NP_001193948.2:n.618+62_618+63insACCTCTCAAAGTGGGCTGGAAGGCCCCG...
NM_002002.5:c.621+62_621+63insACCTCTCAAAGTGGGCTGGAAGGCCCCGAGGACTGGAGACATGTGCCCGGGGCCTT	NP_001993.2:n.621+62_621+63insACCTCTCAAAGTGGGCTGGAAGGCCCCGAGG...