Canonical Allele Identifier: CA2750403371
Gene: MCEE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124381_71124383dup , CM000664.2:g.71124381_71124383dup GRCh38
NC_000002.11:g.71351511_71351513dup , CM000664.1:g.71351511_71351513dup GRCh37
NC_000002.10:g.71205019_71205021dup NCBI36
NG_008977.1:g.10883_10885dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.202_204dup MANE Select ENSP00000244217.5:p.Ile68_Leu69insIle
ENST00000244217.5:c.202_204dup ENSP00000244217.5:p.Ile68_Leu69insIle
ENST00000413592.5:c.70_72dup ENSP00000391140.1:p.Ile24_Leu25insIle
ENST00000486135.1:c.-84_-82dup ENSP00000441569.1:n.-84_-82dup
ENST00000494660.6:c.-84_-82dup ENSP00000437361.1:n.-84_-82dup
NM_032601.3:c.202_204dup NP_115990.3:p.Ile68_Leu69insIle
XM_005264613.2:c.202_204dup XP_005264670.1:p.Ile68_Leu69insIle
XR_939729.1:n.271_273dup
XR_939729.2:n.271_273dup
NM_032601.4:c.202_204dup MANE Select NP_115990.3:p.Ile68_Leu69insIle