Canonical Allele Identifier: CA304904642
Gene: FCER2 HGNC NCBI

Linked Data

dbSNP Id: rs386806491

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7690592_7690599delinsCAGAGGTA , CM000681.2:g.7690592_7690599delinsCAGAGGTA GRCh38
NC_000019.9:g.7755478_7755485delinsCAGAGGTA , CM000681.1:g.7755478_7755485delinsCAGAGGTA GRCh37
NC_000019.8:g.7661478_7661485delinsCAGAGGTA NCBI36
NG_029554.1:g.16548_16555delinsTACCTCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000597921.6:c.470-42_470-35delinsTACCTCTG MANE Select ENSP00000471974.1:n.470-42_470-35delinsTACCTCTG
ENST00000346664.9:c.470-42_470-35delinsTACCTCTG ENSP00000264072.6:n.470-42_470-35delinsTACCTCTG
ENST00000360067.8:c.467-42_467-35delinsTACCTCTG ENSP00000353178.4:n.467-42_467-35delinsTACCTCTG
ENST00000593418.1:c.407-42_407-35delinsTACCTCTG ENSP00000472067.1:n.407-42_407-35delinsTACCTCTG
ENST00000597312.5:n.995-42_995-35delinsTACCTCTG
ENST00000597921.5:c.470-42_470-35delinsTACCTCTG ENSP00000471974.1:n.470-42_470-35delinsTACCTCTG
ENST00000597934.1:n.832-42_832-35delinsTACCTCTG
ENST00000598803.5:n.965-42_965-35delinsTACCTCTG
NM_001207019.2:c.467-42_467-35delinsTACCTCTG NP_001193948.2:n.467-42_467-35delinsTACCTCTG
NM_001220500.1:c.470-42_470-35delinsTACCTCTG NP_001207429.1:n.470-42_470-35delinsTACCTCTG
NM_002002.4:c.470-42_470-35delinsTACCTCTG NP_001993.2:n.470-42_470-35delinsTACCTCTG
XM_005272462.3:c.470-42_470-35delinsTACCTCTG XP_005272519.1:n.470-42_470-35delinsTACCTCTG
XM_005272462.4:c.470-42_470-35delinsTACCTCTG XP_005272519.1:n.470-42_470-35delinsTACCTCTG
NM_001220500.2:c.470-42_470-35delinsTACCTCTG MANE Select NP_001207429.1:n.470-42_470-35delinsTACCTCTG
NM_001207019.3:c.467-42_467-35delinsTACCTCTG NP_001193948.2:n.467-42_467-35delinsTACCTCTG
NM_002002.5:c.470-42_470-35delinsTACCTCTG NP_001993.2:n.470-42_470-35delinsTACCTCTG