Canonical Allele Identifier: CA49696417

Gene: MCEE

Linked Data

• dbSNP Id: rs571877437

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71123963_71123970delinsTAGCCACTGGATT , CM000664.2:g.71123963_71123970delinsTAGCCACTGGATT	GRCh38
NC_000002.11:g.71351093_71351100delinsTAGCCACTGGATT , CM000664.1:g.71351093_71351100delinsTAGCCACTGGATT	GRCh37
NC_000002.10:g.71204601_71204608delinsTAGCCACTGGATT	NCBI36
NG_008977.1:g.11295_11302delinsAATCCAGTGGCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.378+236_378+243delinsAATCCAGTGGCTA MANE Select	ENSP00000244217.5:n.378+236_378+243delinsAATCCAGTGGCTA
ENST00000244217.5:c.378+236_378+243delinsAATCCAGTGGCTA	ENSP00000244217.5:n.378+236_378+243delinsAATCCAGTGGCTA
ENST00000413592.5:c.84+398_84+405delinsAATCCAGTGGCTA	ENSP00000391140.1:n.84+398_84+405delinsAATCCAGTGGCTA
NM_032601.3:c.378+236_378+243delinsAATCCAGTGGCTA	NP_115990.3:n.378+236_378+243delinsAATCCAGTGGCTA
XM_005264613.2:c.216+398_216+405delinsAATCCAGTGGCTA	XP_005264670.1:n.216+398_216+405delinsAATCCAGTGGCTA
XR_939729.1:n.447+236_447+243delinsAATCCAGTGGCTA
XR_939729.2:n.447+236_447+243delinsAATCCAGTGGCTA
NM_032601.4:c.378+236_378+243delinsAATCCAGTGGCTA MANE Select	NP_115990.3:n.378+236_378+243delinsAATCCAGTGGCTA