Canonical Allele Identifier: CA2522352508
Gene: AMELY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.6866662del , CM000686.2:g.6866662del GRCh38
NC_000024.9:g.6734703del , CM000686.1:g.6734703del GRCh37
NC_000024.8:g.6794703del NCBI36
NG_008011.1:g.12366del

Transcript Alleles

HGVS Amino-acid change
ENST00000651267.2:c.574-584del MANE Select ENSP00000498344.1:n.574-584del
ENST00000215479.10:c.574-584del ENSP00000215479.5:n.574-584del
ENST00000651267.1:c.574-584del ENSP00000498344.1:n.574-584del
ENST00000215479.9:c.574-584del ENSP00000215479.5:n.574-584del
ENST00000383036.1:c.616-584del ENSP00000372505.1:n.616-584del
NM_001143.1:c.574-584del NP_001134.1:n.574-584del
XM_011531472.1:c.616-584del XP_011529774.1:n.616-584del
NM_001364814.1:c.616-584del NP_001351743.1:n.616-584del
NM_001143.2:c.574-584del MANE Select NP_001134.1:n.574-584del