Canonical Allele Identifier: CA1259891194
Gene: MCEE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124126_71124127delinsAC , CM000664.2:g.71124126_71124127delinsAC GRCh38
NC_000002.11:g.71351256_71351257delinsAC , CM000664.1:g.71351256_71351257delinsAC GRCh37
NC_000002.10:g.71204764_71204765delinsAC NCBI36
NG_008977.1:g.11138_11139delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.378+79_378+80delinsGT MANE Select ENSP00000244217.5:n.378+79_378+80delinsGT
ENST00000244217.5:c.378+79_378+80delinsGT ENSP00000244217.5:n.378+79_378+80delinsGT
ENST00000413592.5:c.84+241_84+242delinsGT ENSP00000391140.1:n.84+241_84+242delinsGT
NM_032601.3:c.378+79_378+80delinsGT NP_115990.3:n.378+79_378+80delinsGT
XM_005264613.2:c.216+241_216+242delinsGT XP_005264670.1:n.216+241_216+242delinsGT
XR_939729.1:n.447+79_447+80delinsGT
XR_939729.2:n.447+79_447+80delinsGT
NM_032601.4:c.378+79_378+80delinsGT MANE Select NP_115990.3:n.378+79_378+80delinsGT