Canonical Allele Identifier: CA1259891159
Gene: MCEE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124055G= , CM000664.2:g.71124055G= GRCh38
NC_000002.11:g.71351185G= , CM000664.1:g.71351185G= GRCh37
NC_000002.10:g.71204693G= NCBI36
NG_008977.1:g.11210C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.378+151C= MANE Select ENSP00000244217.5:n.378+151C=
ENST00000244217.5:c.378+151C= ENSP00000244217.5:n.378+151C=
ENST00000413592.5:c.84+313C= ENSP00000391140.1:n.84+313C=
NM_032601.3:c.378+151C= NP_115990.3:n.378+151C=
XM_005264613.2:c.216+313C= XP_005264670.1:n.216+313C=
XR_939729.1:n.447+151C=
XR_939729.2:n.447+151C=
NM_032601.4:c.378+151C= MANE Select NP_115990.3:n.378+151C=
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