Canonical Allele Identifier: CA2469903459
Gene: AMELY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.6872512T= , CM000686.2:g.6872512T= GRCh38
NC_000024.9:g.6740553T= , CM000686.1:g.6740553T= GRCh37
NC_000024.8:g.6800553T= NCBI36
NG_008011.1:g.6516A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651267.2:c.54+43A= MANE Select ENSP00000498344.1:n.54+43A=
ENST00000215479.10:c.54+43A= ENSP00000215479.5:n.54+43A=
ENST00000651267.1:c.54+43A= ENSP00000498344.1:n.54+43A=
ENST00000215479.9:c.54+43A= ENSP00000215479.5:n.54+43A=
ENST00000383036.1:c.54+43A= ENSP00000372505.1:n.54+43A=
NM_001143.1:c.54+43A= NP_001134.1:n.54+43A=
XM_011531472.1:c.54+43A= XP_011529774.1:n.54+43A=
NM_001364814.1:c.54+43A= NP_001351743.1:n.54+43A=
NM_001143.2:c.54+43A= MANE Select NP_001134.1:n.54+43A=