Canonical Allele Identifier: CA2321045709

Gene: FCER2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7689956_7690012delinsGAGCCCCTTCCTCTATATCCCCTCCTCCAGGTCAGAGAAGCCTTGGCCAGGTCCCCC , CM000681.2:g.7689956_7690012delinsGAGCCCCTTCCTCTATATCCCCTCCTCCAGGTCAGAGAAGCCTTGGCCAGGTCCCCC	GRCh38
NC_000019.9:g.7754842_7754898delinsGAGCCCCTTCCTCTATATCCCCTCCTCCAGGTCAGAGAAGCCTTGGCCAGGTCCCCC , CM000681.1:g.7754842_7754898delinsGAGCCCCTTCCTCTATATCCCCTCCTCCAGGTCAGAGAAGCCTTGGCCAGGTCCCCC	GRCh37
NC_000019.8:g.7660842_7660898delinsGAGCCCCTTCCTCTATATCCCCTCCTCCAGGTCAGAGAAGCCTTGGCCAGGTCCCCC	NCBI36
NG_029554.1:g.17135_17191delinsGGGGGACCTGGCCAAGGCTTCTCTGACCTGGAGGAGGGGATATAGAGGAAGGGGCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.728+147_728+203delinsGGGGGACCTGGCCAAGGCTTCTCTGACCTGGAGGAGGGGATATAGAGGAAGGGGCTC MANE Select	ENSP00000471974.1:n.728+147_728+203delinsGGGGGACCTGGCCAAGGCTT...
ENST00000346664.9:c.728+147_728+203delinsGGGGGACCTGGCCAAGGCTTCTCTGACCTGGAGGAGGGGATATAGAGGAAGGGGCTC	ENSP00000264072.6:n.728+147_728+203delinsGGGGGACCTGGCCAAGGCTT...
ENST00000360067.8:c.725+147_725+203delinsGGGGGACCTGGCCAAGGCTTCTCTGACCTGGAGGAGGGGATATAGAGGAAGGGGCTC	ENSP00000353178.4:n.725+147_725+203delinsGGGGGACCTGGCCAAGGCTT...
ENST00000597312.5:n.1253+147_1253+203delinsGGGGGACCTGGCCAAGGCTTCTCTGACCTGGAGGAGGGGATATAGAGGAAGGGGCTC
ENST00000597921.5:c.728+147_728+203delinsGGGGGACCTGGCCAAGGCTTCTCTGACCTGGAGGAGGGGATATAGAGGAAGGGGCTC	ENSP00000471974.1:n.728+147_728+203delinsGGGGGACCTGGCCAAGGCTT...
ENST00000597934.1:n.1090+147_1090+203delinsGGGGGACCTGGCCAAGGCTTCTCTGACCTGGAGGAGGGGATATAGAGGAAGGGGCTC
ENST00000598803.5:n.1223+147_1223+203delinsGGGGGACCTGGCCAAGGCTTCTCTGACCTGGAGGAGGGGATATAGAGGAAGGGGCTC
NM_001207019.2:c.725+147_725+203delinsGGGGGACCTGGCCAAGGCTTCTCTGACCTGGAGGAGGGGATATAGAGGAAGGGGCTC	NP_001193948.2:n.725+147_725+203delinsGGGGGACCTGGCCAAGGCTTCTC...
NM_001220500.1:c.728+147_728+203delinsGGGGGACCTGGCCAAGGCTTCTCTGACCTGGAGGAGGGGATATAGAGGAAGGGGCTC	NP_001207429.1:n.728+147_728+203delinsGGGGGACCTGGCCAAGGCTTCTC...
NM_002002.4:c.728+147_728+203delinsGGGGGACCTGGCCAAGGCTTCTCTGACCTGGAGGAGGGGATATAGAGGAAGGGGCTC	NP_001993.2:n.728+147_728+203delinsGGGGGACCTGGCCAAGGCTTCTCTGA...
XM_005272462.3:c.728+147_728+203delinsGGGGGACCTGGCCAAGGCTTCTCTGACCTGGAGGAGGGGATATAGAGGAAGGGGCTC	XP_005272519.1:n.728+147_728+203delinsGGGGGACCTGGCCAAGGCTTCTC...
XM_005272462.4:c.728+147_728+203delinsGGGGGACCTGGCCAAGGCTTCTCTGACCTGGAGGAGGGGATATAGAGGAAGGGGCTC	XP_005272519.1:n.728+147_728+203delinsGGGGGACCTGGCCAAGGCTTCTC...
NM_001220500.2:c.728+147_728+203delinsGGGGGACCTGGCCAAGGCTTCTCTGACCTGGAGGAGGGGATATAGAGGAAGGGGCTC MANE Select	NP_001207429.1:n.728+147_728+203delinsGGGGGACCTGGCCAAGGCTTCTC...
NM_001207019.3:c.725+147_725+203delinsGGGGGACCTGGCCAAGGCTTCTCTGACCTGGAGGAGGGGATATAGAGGAAGGGGCTC	NP_001193948.2:n.725+147_725+203delinsGGGGGACCTGGCCAAGGCTTCTC...
NM_002002.5:c.728+147_728+203delinsGGGGGACCTGGCCAAGGCTTCTCTGACCTGGAGGAGGGGATATAGAGGAAGGGGCTC	NP_001993.2:n.728+147_728+203delinsGGGGGACCTGGCCAAGGCTTCTCTGA...