Canonical Allele Identifier: CA1259891119
Gene: MCEE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71123958T= , CM000664.2:g.71123958T= GRCh38
NC_000002.11:g.71351088T= , CM000664.1:g.71351088T= GRCh37
NC_000002.10:g.71204596T= NCBI36
NG_008977.1:g.11307A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.378+248A= MANE Select ENSP00000244217.5:n.378+248A=
ENST00000244217.5:c.378+248A= ENSP00000244217.5:n.378+248A=
ENST00000413592.5:c.84+410A= ENSP00000391140.1:n.84+410A=
NM_032601.3:c.378+248A= NP_115990.3:n.378+248A=
XM_005264613.2:c.216+410A= XP_005264670.1:n.216+410A=
XR_939729.1:n.447+248A=
XR_939729.2:n.447+248A=
NM_032601.4:c.378+248A= MANE Select NP_115990.3:n.378+248A=
Search 100 bp 5'
Search 100 bp 3'