Canonical Allele Identifier: CA2697552507
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2702030
ClinVar RCV Id: RCV003577163

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94015767del , CM000663.2:g.94015767del GRCh38
NC_000001.10:g.94481323del , CM000663.1:g.94481323del GRCh37
NC_000001.9:g.94253911del NCBI36
NG_009073.1:g.110383del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.5284del MANE Select ENSP00000359245.3:p.Ala1762ProfsTer16
ENST00000370225.3:c.5284del ENSP00000359245.3:p.Ala1762ProfsTer16
ENST00000536513.5:c.1660del ENSP00000439707.2:p.Ala554ProfsTer16
NM_000350.2:c.5284del NP_000341.2:p.Ala1762ProfsTer16
NM_000350.3:c.5284del MANE Select NP_000341.2:p.Ala1762ProfsTer16