Canonical Allele Identifier: CA347185983
Gene: MCEE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124214A>T , CM000664.2:g.71124214A>T GRCh38
NC_000002.11:g.71351344A>T , CM000664.1:g.71351344A>T GRCh37
NC_000002.10:g.71204852A>T NCBI36
NG_008977.1:g.11051T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.370T>A MANE Select ENSP00000244217.5:p.Cys124Ser
ENST00000244217.5:c.370T>A ENSP00000244217.5:p.Cys124Ser
ENST00000413592.5:c.84+154T>A ENSP00000391140.1:n.84+154T>A
ENST00000486135.1:c.85T>A ENSP00000441569.1:p.Cys29Ser
ENST00000494660.6:c.85T>A ENSP00000437361.1:p.Cys29Ser
NM_032601.3:c.370T>A NP_115990.3:p.Cys124Ser
XM_005264613.2:c.216+154T>A XP_005264670.1:n.216+154T>A
XR_939729.1:n.439T>A
XR_939729.2:n.439T>A
NM_032601.4:c.370T>A MANE Select NP_115990.3:p.Cys124Ser