Canonical Allele Identifier: CA414966208
Gene: AMELY HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.6868045C>A , CM000686.2:g.6868045C>A GRCh38
NC_000024.9:g.6736086C>A , CM000686.1:g.6736086C>A GRCh37
NC_000024.8:g.6796086C>A NCBI36
NG_008011.1:g.10983G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000651267.2:c.565G>T MANE Select ENSP00000498344.1:p.Glu189Ter
ENST00000215479.10:c.565G>T ENSP00000215479.5:p.Glu189Ter
ENST00000651267.1:c.565G>T ENSP00000498344.1:p.Glu189Ter
ENST00000215479.9:c.565G>T ENSP00000215479.5:p.Glu189Ter
ENST00000383036.1:c.607G>T ENSP00000372505.1:p.Glu203Ter
NM_001143.1:c.565G>T NP_001134.1:p.Glu189Ter
XM_011531472.1:c.607G>T XP_011529774.1:p.Glu203Ter
NM_001364814.1:c.607G>T NP_001351743.1:p.Glu203Ter
NM_001143.2:c.565G>T MANE Select NP_001134.1:p.Glu189Ter