Canonical Allele Identifier: CA49688182
Gene: MCEE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71110954A>C , CM000664.2:g.71110954A>C GRCh38
NC_000002.11:g.71338084A>C , CM000664.1:g.71338084A>C GRCh37
NC_000002.10:g.71191592A>C NCBI36
NG_008977.1:g.24311T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.379-832T>G MANE Select ENSP00000244217.5:n.379-832T>G
ENST00000244217.5:c.379-832T>G ENSP00000244217.5:n.379-832T>G
ENST00000413592.5:c.85-832T>G ENSP00000391140.1:n.85-832T>G
ENST00000462609.2:n.229-96T>G
NM_032601.3:c.379-832T>G NP_115990.3:n.379-832T>G
XM_005264613.2:c.217-832T>G XP_005264670.1:n.217-832T>G
XR_939729.1:n.448-96T>G
XR_939729.2:n.448-96T>G
NM_032601.4:c.379-832T>G MANE Select NP_115990.3:n.379-832T>G