Canonical Allele Identifier: CA2321045715

Gene: FCER2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7689968_7689969delinsCT , CM000681.2:g.7689968_7689969delinsCT	GRCh38
NC_000019.9:g.7754854_7754855delinsCT , CM000681.1:g.7754854_7754855delinsCT	GRCh37
NC_000019.8:g.7660854_7660855delinsCT	NCBI36
NG_029554.1:g.17178_17179delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.728+190_728+191delinsAG MANE Select	ENSP00000471974.1:n.728+190_728+191delinsAG
ENST00000346664.9:c.728+190_728+191delinsAG	ENSP00000264072.6:n.728+190_728+191delinsAG
ENST00000360067.8:c.725+190_725+191delinsAG	ENSP00000353178.4:n.725+190_725+191delinsAG
ENST00000597312.5:n.1253+190_1253+191delinsAG
ENST00000597921.5:c.728+190_728+191delinsAG	ENSP00000471974.1:n.728+190_728+191delinsAG
ENST00000597934.1:n.1090+190_1090+191delinsAG
ENST00000598803.5:n.1223+190_1223+191delinsAG
NM_001207019.2:c.725+190_725+191delinsAG	NP_001193948.2:n.725+190_725+191delinsAG
NM_001220500.1:c.728+190_728+191delinsAG	NP_001207429.1:n.728+190_728+191delinsAG
NM_002002.4:c.728+190_728+191delinsAG	NP_001993.2:n.728+190_728+191delinsAG
XM_005272462.3:c.728+190_728+191delinsAG	XP_005272519.1:n.728+190_728+191delinsAG
XM_005272462.4:c.728+190_728+191delinsAG	XP_005272519.1:n.728+190_728+191delinsAG
NM_001220500.2:c.728+190_728+191delinsAG MANE Select	NP_001207429.1:n.728+190_728+191delinsAG
NM_001207019.3:c.725+190_725+191delinsAG	NP_001193948.2:n.725+190_725+191delinsAG
NM_002002.5:c.728+190_728+191delinsAG	NP_001993.2:n.728+190_728+191delinsAG