Canonical Allele Identifier: CA414966189
Gene: AMELY HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.6868041T>C , CM000686.2:g.6868041T>C GRCh38
NC_000024.9:g.6736082T>C , CM000686.1:g.6736082T>C GRCh37
NC_000024.8:g.6796082T>C NCBI36
NG_008011.1:g.10987A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651267.2:c.569A>G MANE Select ENSP00000498344.1:p.Glu190Gly
ENST00000215479.10:c.569A>G ENSP00000215479.5:p.Glu190Gly
ENST00000651267.1:c.569A>G ENSP00000498344.1:p.Glu190Gly
ENST00000215479.9:c.569A>G ENSP00000215479.5:p.Glu190Gly
ENST00000383036.1:c.611A>G ENSP00000372505.1:p.Glu204Gly
NM_001143.1:c.569A>G NP_001134.1:p.Glu190Gly
XM_011531472.1:c.611A>G XP_011529774.1:p.Glu204Gly
NM_001364814.1:c.611A>G NP_001351743.1:p.Glu204Gly
NM_001143.2:c.569A>G MANE Select NP_001134.1:p.Glu190Gly