Canonical Allele Identifier: CA1259891330
Gene: MCEE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124456C= , CM000664.2:g.71124456C= GRCh38
NC_000002.11:g.71351586C= , CM000664.1:g.71351586C= GRCh37
NC_000002.10:g.71205094C= NCBI36
NG_008977.1:g.10809G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.128G= MANE Select ENSP00000244217.5:p.Trp43=
ENST00000244217.5:c.128G= ENSP00000244217.5:p.Trp43=
ENST00000486135.1:c.-158G= ENSP00000441569.1:n.-158G=
ENST00000494660.6:c.-158G= ENSP00000437361.1:n.-158G=
NM_032601.3:c.128G= NP_115990.3:p.Trp43=
XM_005264613.2:c.128G= XP_005264670.1:p.Trp43=
XR_939729.1:n.197G=
XR_939729.2:n.197G=
NM_032601.4:c.128G= MANE Select NP_115990.3:p.Trp43=