Canonical Allele Identifier: CA645372188
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2202790
ClinVar RCV Id: RCV002648171

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94041338_94041339delinsC , CM000663.2:g.94041338_94041339delinsC GRCh38
NC_000001.10:g.94506894_94506895delinsC , CM000663.1:g.94506894_94506895delinsC GRCh37
NC_000001.9:g.94279482_94279483delinsC NCBI36
NG_009073.1:g.84811_84812delinsG

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.3392_3393delinsG MANE Select ENSP00000359245.3:p.Ala1131GlyfsTer17
ENST00000370225.3:c.3392_3393delinsG ENSP00000359245.3:p.Ala1131GlyfsTer17
ENST00000536513.5:c.-64-1250_-64-1249delinsG ENSP00000439707.2:n.-64-1250_-64-1249deli...
NM_000350.2:c.3392_3393delinsG NP_000341.2:p.Ala1131GlyfsTer17
NM_000350.3:c.3392_3393delinsG MANE Select NP_000341.2:p.Ala1131GlyfsTer17