Canonical Allele Identifier: CA2659522943
Gene: MCEE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124592del , CM000664.2:g.71124592del GRCh38
NC_000002.11:g.71351722del , CM000664.1:g.71351722del GRCh37
NC_000002.10:g.71205230del NCBI36
NG_008977.1:g.10673del

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.41-49del MANE Select ENSP00000244217.5:n.41-49del
ENST00000244217.5:c.41-49del ENSP00000244217.5:n.41-49del
ENST00000486135.1:c.-245-49del ENSP00000441569.1:n.-245-49del
ENST00000494660.6:c.-245-49del ENSP00000437361.1:n.-245-49del
NM_032601.3:c.41-49del NP_115990.3:n.41-49del
XM_005264613.2:c.41-49del XP_005264670.1:n.41-49del
XR_939729.1:n.110-49del
XR_939729.2:n.110-49del
NM_032601.4:c.41-49del MANE Select NP_115990.3:n.41-49del