Canonical Allele Identifier: CA1259891114
Gene: MCEE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71123949T= , CM000664.2:g.71123949T= GRCh38
NC_000002.11:g.71351079T= , CM000664.1:g.71351079T= GRCh37
NC_000002.10:g.71204587T= NCBI36
NG_008977.1:g.11316A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.378+257A= MANE Select ENSP00000244217.5:n.378+257A=
ENST00000244217.5:c.378+257A= ENSP00000244217.5:n.378+257A=
ENST00000413592.5:c.84+419A= ENSP00000391140.1:n.84+419A=
NM_032601.3:c.378+257A= NP_115990.3:n.378+257A=
XM_005264613.2:c.216+419A= XP_005264670.1:n.216+419A=
XR_939729.1:n.447+257A=
XR_939729.2:n.447+257A=
NM_032601.4:c.378+257A= MANE Select NP_115990.3:n.378+257A=
Search 100 bp 5'
Search 100 bp 3'