Canonical Allele Identifier: CA2587988845

Gene: FCER2

Linked Data

• gnomAD v4: 19-7690232-AGCCGGTGTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690235_7690243del , CM000681.2:g.7690235_7690243del	GRCh38
NC_000019.9:g.7755121_7755129del , CM000681.1:g.7755121_7755129del	GRCh37
NC_000019.8:g.7661121_7661129del	NCBI36
NG_029554.1:g.16906_16914del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.646_654del MANE Select	ENSP00000471974.1:p.His216_Gly218del
ENST00000346664.9:c.646_654del	ENSP00000264072.6:p.His216_Gly218del
ENST00000360067.8:c.643_651del	ENSP00000353178.4:p.His215_Gly217del
ENST00000597312.5:n.1171_1179del
ENST00000597921.5:c.646_654del	ENSP00000471974.1:p.His216_Gly218del
ENST00000597934.1:n.1008_1016del
ENST00000598803.5:n.1141_1149del
NM_001207019.2:c.643_651del	NP_001193948.2:p.His215_Gly217del
NM_001220500.1:c.646_654del	NP_001207429.1:p.His216_Gly218del
NM_002002.4:c.646_654del	NP_001993.2:p.His216_Gly218del
XM_005272462.3:c.646_654del	XP_005272519.1:p.His216_Gly218del
XM_005272462.4:c.646_654del	XP_005272519.1:p.His216_Gly218del
NM_001220500.2:c.646_654del MANE Select	NP_001207429.1:p.His216_Gly218del
NM_001207019.3:c.643_651del	NP_001193948.2:p.His215_Gly217del
NM_002002.5:c.646_654del	NP_001993.2:p.His216_Gly218del