Canonical Allele Identifier: CA1259891179
Gene: MCEE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124085A= , CM000664.2:g.71124085A= GRCh38
NC_000002.11:g.71351215A= , CM000664.1:g.71351215A= GRCh37
NC_000002.10:g.71204723A= NCBI36
NG_008977.1:g.11180T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.378+121T= MANE Select ENSP00000244217.5:n.378+121T=
ENST00000244217.5:c.378+121T= ENSP00000244217.5:n.378+121T=
ENST00000413592.5:c.84+283T= ENSP00000391140.1:n.84+283T=
NM_032601.3:c.378+121T= NP_115990.3:n.378+121T=
XM_005264613.2:c.216+283T= XP_005264670.1:n.216+283T=
XR_939729.1:n.447+121T=
XR_939729.2:n.447+121T=
NM_032601.4:c.378+121T= MANE Select NP_115990.3:n.378+121T=
Search 100 bp 5'
Search 100 bp 3'