Canonical Allele Identifier: CA1259891327
Gene: MCEE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124452G= , CM000664.2:g.71124452G= GRCh38
NC_000002.11:g.71351582G= , CM000664.1:g.71351582G= GRCh37
NC_000002.10:g.71205090G= NCBI36
NG_008977.1:g.10813C=

Transcript Alleles

HGVS Amino-acid change
ENST00000244217.6:c.132C= MANE Select ENSP00000244217.5:p.Asn44=
ENST00000244217.5:c.132C= ENSP00000244217.5:p.Asn44=
ENST00000486135.1:c.-154C= ENSP00000441569.1:n.-154C=
ENST00000494660.6:c.-154C= ENSP00000437361.1:n.-154C=
NM_032601.3:c.132C= NP_115990.3:p.Asn44=
XM_005264613.2:c.132C= XP_005264670.1:p.Asn44=
XR_939729.1:n.201C=
XR_939729.2:n.201C=
NM_032601.4:c.132C= MANE Select NP_115990.3:p.Asn44=
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