Canonical Allele Identifier: CA1259891385
Gene: MCEE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124584T= , CM000664.2:g.71124584T= GRCh38
NC_000002.11:g.71351714T= , CM000664.1:g.71351714T= GRCh37
NC_000002.10:g.71205222T= NCBI36
NG_008977.1:g.10681A=

Transcript Alleles

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