Canonical Allele Identifier: CA1259891334
Gene: MCEE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124462G= , CM000664.2:g.71124462G= GRCh38
NC_000002.11:g.71351592G= , CM000664.1:g.71351592G= GRCh37
NC_000002.10:g.71205100G= NCBI36
NG_008977.1:g.10803C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.122C= MANE Select ENSP00000244217.5:p.Ser41=
ENST00000244217.5:c.122C= ENSP00000244217.5:p.Ser41=
ENST00000486135.1:c.-164C= ENSP00000441569.1:n.-164C=
ENST00000494660.6:c.-164C= ENSP00000437361.1:n.-164C=
NM_032601.3:c.122C= NP_115990.3:p.Ser41=
XM_005264613.2:c.122C= XP_005264670.1:p.Ser41=
XR_939729.1:n.191C=
XR_939729.2:n.191C=
NM_032601.4:c.122C= MANE Select NP_115990.3:p.Ser41=