Canonical Allele Identifier: CA1138819769
Gene: AMELY HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.6866662_6866669del , CM000686.2:g.6866662_6866669del GRCh38
NC_000024.9:g.6734703_6734710del , CM000686.1:g.6734703_6734710del GRCh37
NC_000024.8:g.6794703_6794710del NCBI36
NG_008011.1:g.12360_12367del

Transcript Alleles

HGVS Amino-acid change
ENST00000651267.2:c.574-590_574-583del MANE Select ENSP00000498344.1:n.574-590_574-583del
ENST00000215479.10:c.574-590_574-583del ENSP00000215479.5:n.574-590_574-583del
ENST00000651267.1:c.574-590_574-583del ENSP00000498344.1:n.574-590_574-583del
ENST00000215479.9:c.574-590_574-583del ENSP00000215479.5:n.574-590_574-583del
ENST00000383036.1:c.616-590_616-583del ENSP00000372505.1:n.616-590_616-583del
NM_001143.1:c.574-590_574-583del NP_001134.1:n.574-590_574-583del
XM_011531472.1:c.616-590_616-583del XP_011529774.1:n.616-590_616-583del
NM_001364814.1:c.616-590_616-583del NP_001351743.1:n.616-590_616-583del
NM_001143.2:c.574-590_574-583del MANE Select NP_001134.1:n.574-590_574-583del