Canonical Allele Identifier: CA2646650966
Gene: ABCA4 HGNC NCBI

Linked Data

gnomAD v4: 1-94056555-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94056557del , CM000663.2:g.94056557del GRCh38
NC_000001.10:g.94522113del , CM000663.1:g.94522113del GRCh37
NC_000001.9:g.94294701del NCBI36
NG_009073.1:g.69594del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2382+45del MANE Select ENSP00000359245.3:n.2382+45del
ENST00000649773.1:c.2161-1241del ENSP00000496882.1:n.2161-1241del
ENST00000370225.3:c.2382+45del ENSP00000359245.3:n.2382+45del
ENST00000536513.5:c.-65+6618del ENSP00000439707.2:n.-65+6618del
NM_000350.2:c.2382+45del NP_000341.2:n.2382+45del
NM_000350.3:c.2382+45del MANE Select NP_000341.2:n.2382+45del
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