Canonical Allele Identifier: CA1138822768
Gene: AMELY HGNC NCBI

Linked Data

gnomAD v3: Y-6872478-T-A
gnomAD v4: Y-6872478-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.6872478T>A , CM000686.2:g.6872478T>A GRCh38
NC_000024.9:g.6740519T>A , CM000686.1:g.6740519T>A GRCh37
NC_000024.8:g.6800519T>A NCBI36
NG_008011.1:g.6550A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651267.2:c.54+77A>T MANE Select ENSP00000498344.1:n.54+77A>T
ENST00000215479.10:c.54+77A>T ENSP00000215479.5:n.54+77A>T
ENST00000651267.1:c.54+77A>T ENSP00000498344.1:n.54+77A>T
ENST00000215479.9:c.54+77A>T ENSP00000215479.5:n.54+77A>T
ENST00000383036.1:c.54+77A>T ENSP00000372505.1:n.54+77A>T
NM_001143.1:c.54+77A>T NP_001134.1:n.54+77A>T
XM_011531472.1:c.54+77A>T XP_011529774.1:n.54+77A>T
NM_001364814.1:c.54+77A>T NP_001351743.1:n.54+77A>T
NM_001143.2:c.54+77A>T MANE Select NP_001134.1:n.54+77A>T