Canonical Allele Identifier: CA414966182
Gene: AMELY HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.6868040T>A , CM000686.2:g.6868040T>A GRCh38
NC_000024.9:g.6736081T>A , CM000686.1:g.6736081T>A GRCh37
NC_000024.8:g.6796081T>A NCBI36
NG_008011.1:g.10988A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000651267.2:c.570A>T MANE Select ENSP00000498344.1:p.Glu190Asp
ENST00000215479.10:c.570A>T ENSP00000215479.5:p.Glu190Asp
ENST00000651267.1:c.570A>T ENSP00000498344.1:p.Glu190Asp
ENST00000215479.9:c.570A>T ENSP00000215479.5:p.Glu190Asp
ENST00000383036.1:c.612A>T ENSP00000372505.1:p.Glu204Asp
NM_001143.1:c.570A>T NP_001134.1:p.Glu190Asp
XM_011531472.1:c.612A>T XP_011529774.1:p.Glu204Asp
NM_001364814.1:c.612A>T NP_001351743.1:p.Glu204Asp
NM_001143.2:c.570A>T MANE Select NP_001134.1:p.Glu190Asp