Canonical Allele Identifier: CA920050684

Gene: FCER2

Linked Data

• dbSNP Id: rs1599432065

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690590_7690591insCAG , CM000681.2:g.7690590_7690591insCAG	GRCh38
NC_000019.9:g.7755476_7755477insCAG , CM000681.1:g.7755476_7755477insCAG	GRCh37
NC_000019.8:g.7661476_7661477insCAG	NCBI36
NG_029554.1:g.16556_16557insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.470-34_470-33insCTG MANE Select	ENSP00000471974.1:n.470-34_470-33insCTG
ENST00000346664.9:c.470-34_470-33insCTG	ENSP00000264072.6:n.470-34_470-33insCTG
ENST00000360067.8:c.467-34_467-33insCTG	ENSP00000353178.4:n.467-34_467-33insCTG
ENST00000593418.1:c.407-34_407-33insCTG	ENSP00000472067.1:n.407-34_407-33insCTG
ENST00000597312.5:n.995-34_995-33insCTG
ENST00000597921.5:c.470-34_470-33insCTG	ENSP00000471974.1:n.470-34_470-33insCTG
ENST00000597934.1:n.832-34_832-33insCTG
ENST00000598803.5:n.965-34_965-33insCTG
NM_001207019.2:c.467-34_467-33insCTG	NP_001193948.2:n.467-34_467-33insCTG
NM_001220500.1:c.470-34_470-33insCTG	NP_001207429.1:n.470-34_470-33insCTG
NM_002002.4:c.470-34_470-33insCTG	NP_001993.2:n.470-34_470-33insCTG
XM_005272462.3:c.470-34_470-33insCTG	XP_005272519.1:n.470-34_470-33insCTG
XM_005272462.4:c.470-34_470-33insCTG	XP_005272519.1:n.470-34_470-33insCTG
NM_001220500.2:c.470-34_470-33insCTG MANE Select	NP_001207429.1:n.470-34_470-33insCTG
NM_001207019.3:c.467-34_467-33insCTG	NP_001193948.2:n.467-34_467-33insCTG
NM_002002.5:c.470-34_470-33insCTG	NP_001993.2:n.470-34_470-33insCTG