Canonical Allele Identifier: CA1259891379
Gene: MCEE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124571C= , CM000664.2:g.71124571C= GRCh38
NC_000002.11:g.71351701C= , CM000664.1:g.71351701C= GRCh37
NC_000002.10:g.71205209C= NCBI36
NG_008977.1:g.10694G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.41-28G= MANE Select ENSP00000244217.5:n.41-28G=
ENST00000244217.5:c.41-28G= ENSP00000244217.5:n.41-28G=
ENST00000486135.1:c.-245-28G= ENSP00000441569.1:n.-245-28G=
ENST00000494660.6:c.-245-28G= ENSP00000437361.1:n.-245-28G=
NM_032601.3:c.41-28G= NP_115990.3:n.41-28G=
XM_005264613.2:c.41-28G= XP_005264670.1:n.41-28G=
XR_939729.1:n.110-28G=
XR_939729.2:n.110-28G=
NM_032601.4:c.41-28G= MANE Select NP_115990.3:n.41-28G=
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