Canonical Allele Identifier: CA414966218
Gene: AMELY HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.6868047T>A , CM000686.2:g.6868047T>A GRCh38
NC_000024.9:g.6736088T>A , CM000686.1:g.6736088T>A GRCh37
NC_000024.8:g.6796088T>A NCBI36
NG_008011.1:g.10981A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000651267.2:c.563A>T MANE Select ENSP00000498344.1:p.Gln188Leu
ENST00000215479.10:c.563A>T ENSP00000215479.5:p.Gln188Leu
ENST00000651267.1:c.563A>T ENSP00000498344.1:p.Gln188Leu
ENST00000215479.9:c.563A>T ENSP00000215479.5:p.Gln188Leu
ENST00000383036.1:c.605A>T ENSP00000372505.1:p.Gln202Leu
NM_001143.1:c.563A>T NP_001134.1:p.Gln188Leu
XM_011531472.1:c.605A>T XP_011529774.1:p.Gln202Leu
NM_001364814.1:c.605A>T NP_001351743.1:p.Gln202Leu
NM_001143.2:c.563A>T MANE Select NP_001134.1:p.Gln188Leu