Canonical Allele Identifier: CA1259891126
Gene: MCEE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71123962_71123970delinsTGGCACTTA , CM000664.2:g.71123962_71123970delinsTGGCACTTA GRCh38
NC_000002.11:g.71351092_71351100delinsTGGCACTTA , CM000664.1:g.71351092_71351100delinsTGGCACTTA GRCh37
NC_000002.10:g.71204600_71204608delinsTGGCACTTA NCBI36
NG_008977.1:g.11295_11303delinsTAAGTGCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.378+236_378+244delinsTAAGTGCCA MANE Select ENSP00000244217.5:n.378+236_378+244delinsTAAGTGCCA
ENST00000244217.5:c.378+236_378+244delinsTAAGTGCCA ENSP00000244217.5:n.378+236_378+244delinsTAAGTGCCA
ENST00000413592.5:c.84+398_84+406delinsTAAGTGCCA ENSP00000391140.1:n.84+398_84+406delinsTAAGTGCCA
NM_032601.3:c.378+236_378+244delinsTAAGTGCCA NP_115990.3:n.378+236_378+244delinsTAAGTGCCA
XM_005264613.2:c.216+398_216+406delinsTAAGTGCCA XP_005264670.1:n.216+398_216+406delinsTAAGTGCCA
XR_939729.1:n.447+236_447+244delinsTAAGTGCCA
XR_939729.2:n.447+236_447+244delinsTAAGTGCCA
NM_032601.4:c.378+236_378+244delinsTAAGTGCCA MANE Select NP_115990.3:n.378+236_378+244delinsTAAGTGCCA