Canonical Allele Identifier: CA1259891223
Gene: MCEE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124191A= , CM000664.2:g.71124191A= GRCh38
NC_000002.11:g.71351321A= , CM000664.1:g.71351321A= GRCh37
NC_000002.10:g.71204829A= NCBI36
NG_008977.1:g.11074T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.378+15T= MANE Select ENSP00000244217.5:n.378+15T=
ENST00000244217.5:c.378+15T= ENSP00000244217.5:n.378+15T=
ENST00000413592.5:c.84+177T= ENSP00000391140.1:n.84+177T=
NM_032601.3:c.378+15T= NP_115990.3:n.378+15T=
XM_005264613.2:c.216+177T= XP_005264670.1:n.216+177T=
XR_939729.1:n.447+15T=
XR_939729.2:n.447+15T=
NM_032601.4:c.378+15T= MANE Select NP_115990.3:n.378+15T=