Canonical Allele Identifier: CA2750403370
Gene: MCEE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124377dup , CM000664.2:g.71124377dup GRCh38
NC_000002.11:g.71351507dup , CM000664.1:g.71351507dup GRCh37
NC_000002.10:g.71205015dup NCBI36
NG_008977.1:g.10892dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.211dup MANE Select ENSP00000244217.5:p.Ala71GlyfsTer5
ENST00000244217.5:c.211dup ENSP00000244217.5:p.Ala71GlyfsTer5
ENST00000413592.5:c.79dup ENSP00000391140.1:p.Ala27GlyfsTer5
ENST00000486135.1:c.-75dup ENSP00000441569.1:n.-75dup
ENST00000494660.6:c.-75dup ENSP00000437361.1:n.-75dup
NM_032601.3:c.211dup NP_115990.3:p.Ala71GlyfsTer5
XM_005264613.2:c.211dup XP_005264670.1:p.Ala71GlyfsTer5
XR_939729.1:n.280dup
XR_939729.2:n.280dup
NM_032601.4:c.211dup MANE Select NP_115990.3:p.Ala71GlyfsTer5