Canonical Allele Identifier: CA2569309195
Gene: AMELY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.6866638dup , CM000686.2:g.6866638dup GRCh38
NC_000024.9:g.6734679dup , CM000686.1:g.6734679dup GRCh37
NC_000024.8:g.6794679dup NCBI36
NG_008011.1:g.12392dup

Transcript Alleles

HGVS Amino-acid change
ENST00000651267.2:c.574-558dup MANE Select ENSP00000498344.1:n.574-558dup
ENST00000215479.10:c.574-558dup ENSP00000215479.5:n.574-558dup
ENST00000651267.1:c.574-558dup ENSP00000498344.1:n.574-558dup
ENST00000215479.9:c.574-558dup ENSP00000215479.5:n.574-558dup
ENST00000383036.1:c.616-558dup ENSP00000372505.1:n.616-558dup
NM_001143.1:c.574-558dup NP_001134.1:n.574-558dup
XM_011531472.1:c.616-558dup XP_011529774.1:n.616-558dup
NM_001364814.1:c.616-558dup NP_001351743.1:n.616-558dup
NM_001143.2:c.574-558dup MANE Select NP_001134.1:n.574-558dup