Canonical Allele Identifier: CA1259891335
Gene: MCEE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124464A= , CM000664.2:g.71124464A= GRCh38
NC_000002.11:g.71351594A= , CM000664.1:g.71351594A= GRCh37
NC_000002.10:g.71205102A= NCBI36
NG_008977.1:g.10801T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.120T= MANE Select ENSP00000244217.5:p.Gly40=
ENST00000244217.5:c.120T= ENSP00000244217.5:p.Gly40=
ENST00000486135.1:c.-166T= ENSP00000441569.1:n.-166T=
ENST00000494660.6:c.-166T= ENSP00000437361.1:n.-166T=
NM_032601.3:c.120T= NP_115990.3:p.Gly40=
XM_005264613.2:c.120T= XP_005264670.1:p.Gly40=
XR_939729.1:n.189T=
XR_939729.2:n.189T=
NM_032601.4:c.120T= MANE Select NP_115990.3:p.Gly40=