Canonical Allele Identifier: CA2321046022

Gene: FCER2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690577_7690578delinsCG , CM000681.2:g.7690577_7690578delinsCG	GRCh38
NC_000019.9:g.7755463_7755464delinsCG , CM000681.1:g.7755463_7755464delinsCG	GRCh37
NC_000019.8:g.7661463_7661464delinsCG	NCBI36
NG_029554.1:g.16569_16570delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.470-21_470-20delinsCG MANE Select	ENSP00000471974.1:n.470-21_470-20delinsCG
ENST00000346664.9:c.470-21_470-20delinsCG	ENSP00000264072.6:n.470-21_470-20delinsCG
ENST00000360067.8:c.467-21_467-20delinsCG	ENSP00000353178.4:n.467-21_467-20delinsCG
ENST00000593418.1:c.407-21_407-20delinsCG	ENSP00000472067.1:n.407-21_407-20delinsCG
ENST00000597312.5:n.995-21_995-20delinsCG
ENST00000597921.5:c.470-21_470-20delinsCG	ENSP00000471974.1:n.470-21_470-20delinsCG
ENST00000597934.1:n.832-21_832-20delinsCG
ENST00000598803.5:n.965-21_965-20delinsCG
NM_001207019.2:c.467-21_467-20delinsCG	NP_001193948.2:n.467-21_467-20delinsCG
NM_001220500.1:c.470-21_470-20delinsCG	NP_001207429.1:n.470-21_470-20delinsCG
NM_002002.4:c.470-21_470-20delinsCG	NP_001993.2:n.470-21_470-20delinsCG
XM_005272462.3:c.470-21_470-20delinsCG	XP_005272519.1:n.470-21_470-20delinsCG
XM_005272462.4:c.470-21_470-20delinsCG	XP_005272519.1:n.470-21_470-20delinsCG
NM_001220500.2:c.470-21_470-20delinsCG MANE Select	NP_001207429.1:n.470-21_470-20delinsCG
NM_001207019.3:c.467-21_467-20delinsCG	NP_001193948.2:n.467-21_467-20delinsCG
NM_002002.5:c.470-21_470-20delinsCG	NP_001993.2:n.470-21_470-20delinsCG