Canonical Allele Identifier: CA1259891323
Gene: MCEE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124445G= , CM000664.2:g.71124445G= GRCh38
NC_000002.11:g.71351575G= , CM000664.1:g.71351575G= GRCh37
NC_000002.10:g.71205083G= NCBI36
NG_008977.1:g.10820C=

Transcript Alleles

HGVS Amino-acid change
ENST00000244217.6:c.139C= MANE Select ENSP00000244217.5:p.Arg47=
ENST00000244217.5:c.139C= ENSP00000244217.5:p.Arg47=
ENST00000413592.5:c.7C= ENSP00000391140.1:p.Arg3=
ENST00000486135.1:c.-147C= ENSP00000441569.1:n.-147C=
ENST00000494660.6:c.-147C= ENSP00000437361.1:n.-147C=
NM_032601.3:c.139C= NP_115990.3:p.Arg47=
XM_005264613.2:c.139C= XP_005264670.1:p.Arg47=
XR_939729.1:n.208C=
XR_939729.2:n.208C=
NM_032601.4:c.139C= MANE Select NP_115990.3:p.Arg47=