Canonical Allele Identifier: CA1181402687
Gene: ABCA4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94007553T= , CM000663.2:g.94007553T= GRCh38
NC_000001.10:g.94473109T= , CM000663.1:g.94473109T= GRCh37
NC_000001.9:g.94245697T= NCBI36
NG_009073.1:g.118597A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.6005+81A= MANE Select ENSP00000359245.3:n.6005+81A=
ENST00000370225.3:c.6005+81A= ENSP00000359245.3:n.6005+81A=
ENST00000465352.1:n.421+81A=
ENST00000484388.1:n.119+81A=
ENST00000536513.5:c.2381+81A= ENSP00000439707.2:n.2381+81A=
NM_000350.2:c.6005+81A= NP_000341.2:n.6005+81A=
NM_000350.3:c.6005+81A= MANE Select NP_000341.2:n.6005+81A=
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