Canonical Allele Identifier: CA1259891146
Gene: MCEE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124034G= , CM000664.2:g.71124034G= GRCh38
NC_000002.11:g.71351164G= , CM000664.1:g.71351164G= GRCh37
NC_000002.10:g.71204672G= NCBI36
NG_008977.1:g.11231C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.378+172C= MANE Select ENSP00000244217.5:n.378+172C=
ENST00000244217.5:c.378+172C= ENSP00000244217.5:n.378+172C=
ENST00000413592.5:c.84+334C= ENSP00000391140.1:n.84+334C=
NM_032601.3:c.378+172C= NP_115990.3:n.378+172C=
XM_005264613.2:c.216+334C= XP_005264670.1:n.216+334C=
XR_939729.1:n.447+172C=
XR_939729.2:n.447+172C=
NM_032601.4:c.378+172C= MANE Select NP_115990.3:n.378+172C=