Canonical Allele Identifier: CA2321046054

Gene: FCER2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690599_7690608delinsGCCTTGGGCA , CM000681.2:g.7690599_7690608delinsGCCTTGGGCA	GRCh38
NC_000019.9:g.7755485_7755494delinsGCCTTGGGCA , CM000681.1:g.7755485_7755494delinsGCCTTGGGCA	GRCh37
NC_000019.8:g.7661485_7661494delinsGCCTTGGGCA	NCBI36
NG_029554.1:g.16539_16548delinsTGCCCAAGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.470-51_470-42delinsTGCCCAAGGC MANE Select	ENSP00000471974.1:n.470-51_470-42delinsTGCCCAAGGC
ENST00000346664.9:c.470-51_470-42delinsTGCCCAAGGC	ENSP00000264072.6:n.470-51_470-42delinsTGCCCAAGGC
ENST00000360067.8:c.467-51_467-42delinsTGCCCAAGGC	ENSP00000353178.4:n.467-51_467-42delinsTGCCCAAGGC
ENST00000593418.1:c.407-51_407-42delinsTGCCCAAGGC	ENSP00000472067.1:n.407-51_407-42delinsTGCCCAAGGC
ENST00000597312.5:n.995-51_995-42delinsTGCCCAAGGC
ENST00000597921.5:c.470-51_470-42delinsTGCCCAAGGC	ENSP00000471974.1:n.470-51_470-42delinsTGCCCAAGGC
ENST00000597934.1:n.832-51_832-42delinsTGCCCAAGGC
ENST00000598803.5:n.965-51_965-42delinsTGCCCAAGGC
NM_001207019.2:c.467-51_467-42delinsTGCCCAAGGC	NP_001193948.2:n.467-51_467-42delinsTGCCCAAGGC
NM_001220500.1:c.470-51_470-42delinsTGCCCAAGGC	NP_001207429.1:n.470-51_470-42delinsTGCCCAAGGC
NM_002002.4:c.470-51_470-42delinsTGCCCAAGGC	NP_001993.2:n.470-51_470-42delinsTGCCCAAGGC
XM_005272462.3:c.470-51_470-42delinsTGCCCAAGGC	XP_005272519.1:n.470-51_470-42delinsTGCCCAAGGC
XM_005272462.4:c.470-51_470-42delinsTGCCCAAGGC	XP_005272519.1:n.470-51_470-42delinsTGCCCAAGGC
NM_001220500.2:c.470-51_470-42delinsTGCCCAAGGC MANE Select	NP_001207429.1:n.470-51_470-42delinsTGCCCAAGGC
NM_001207019.3:c.467-51_467-42delinsTGCCCAAGGC	NP_001193948.2:n.467-51_467-42delinsTGCCCAAGGC
NM_002002.5:c.470-51_470-42delinsTGCCCAAGGC	NP_001993.2:n.470-51_470-42delinsTGCCCAAGGC