Canonical Allele Identifier: CA1259891303
Gene: MCEE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124404C= , CM000664.2:g.71124404C= GRCh38
NC_000002.11:g.71351534C= , CM000664.1:g.71351534C= GRCh37
NC_000002.10:g.71205042C= NCBI36
NG_008977.1:g.10861G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.180G= MANE Select ENSP00000244217.5:p.Lys60=
ENST00000244217.5:c.180G= ENSP00000244217.5:p.Lys60=
ENST00000413592.5:c.48G= ENSP00000391140.1:p.Lys16=
ENST00000486135.1:c.-106G= ENSP00000441569.1:n.-106G=
ENST00000494660.6:c.-106G= ENSP00000437361.1:n.-106G=
NM_032601.3:c.180G= NP_115990.3:p.Lys60=
XM_005264613.2:c.180G= XP_005264670.1:p.Lys60=
XR_939729.1:n.249G=
XR_939729.2:n.249G=
NM_032601.4:c.180G= MANE Select NP_115990.3:p.Lys60=