Canonical Allele Identifier: CA347189648
Gene: MCEE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124487G>T , CM000664.2:g.71124487G>T GRCh38
NC_000002.11:g.71351617G>T , CM000664.1:g.71351617G>T GRCh37
NC_000002.10:g.71205125G>T NCBI36
NG_008977.1:g.10778C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.97C>A MANE Select ENSP00000244217.5:p.Gln33Lys
ENST00000244217.5:c.97C>A ENSP00000244217.5:p.Gln33Lys
ENST00000486135.1:c.-189C>A ENSP00000441569.1:n.-189C>A
ENST00000494660.6:c.-189C>A ENSP00000437361.1:n.-189C>A
NM_032601.3:c.97C>A NP_115990.3:p.Gln33Lys
XM_005264613.2:c.97C>A XP_005264670.1:p.Gln33Lys
XR_939729.1:n.166C>A
XR_939729.2:n.166C>A
NM_032601.4:c.97C>A MANE Select NP_115990.3:p.Gln33Lys