Canonical Allele Identifier: CA993173857
Gene: FCER2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7690597_7690600del , CM000681.2:g.7690597_7690600del GRCh38
NC_000019.9:g.7755483_7755486del , CM000681.1:g.7755483_7755486del GRCh37
NC_000019.8:g.7661483_7661486del NCBI36
NG_029554.1:g.16547_16550del

Transcript Alleles

HGVS Amino-acid Change
ENST00000597921.6:c.470-43_470-40del MANE Select ENSP00000471974.1:n.470-43_470-40del
ENST00000346664.9:c.470-43_470-40del ENSP00000264072.6:n.470-43_470-40del
ENST00000360067.8:c.467-43_467-40del ENSP00000353178.4:n.467-43_467-40del
ENST00000593418.1:c.407-43_407-40del ENSP00000472067.1:n.407-43_407-40del
ENST00000597312.5:n.995-43_995-40del
ENST00000597921.5:c.470-43_470-40del ENSP00000471974.1:n.470-43_470-40del
ENST00000597934.1:n.832-43_832-40del
ENST00000598803.5:n.965-43_965-40del
NM_001207019.2:c.467-43_467-40del NP_001193948.2:n.467-43_467-40del
NM_001220500.1:c.470-43_470-40del NP_001207429.1:n.470-43_470-40del
NM_002002.4:c.470-43_470-40del NP_001993.2:n.470-43_470-40del
XM_005272462.3:c.470-43_470-40del XP_005272519.1:n.470-43_470-40del
XM_005272462.4:c.470-43_470-40del XP_005272519.1:n.470-43_470-40del
NM_001220500.2:c.470-43_470-40del MANE Select NP_001207429.1:n.470-43_470-40del
NM_001207019.3:c.467-43_467-40del NP_001193948.2:n.467-43_467-40del
NM_002002.5:c.470-43_470-40del NP_001993.2:n.470-43_470-40del