Canonical Allele Identifier: CA2744618334
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94047163_94047164insAGT , CM000663.2:g.94047163_94047164insAGT GRCh38
NC_000001.10:g.94512719_94512720insAGT , CM000663.1:g.94512719_94512720insAGT GRCh37
NC_000001.9:g.94285307_94285308insAGT NCBI36
NG_009073.1:g.78986_78987insACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2744-71_2744-70insACT MANE Select ENSP00000359245.3:n.2744-71_2744-70insACT
ENST00000649773.1:c.2522-71_2522-70insACT ENSP00000496882.1:n.2522-71_2522-70insACT
ENST00000370225.3:c.2744-71_2744-70insACT ENSP00000359245.3:n.2744-71_2744-70insACT
ENST00000536513.5:c.-64-7075_-64-7074insACT ENSP00000439707.2:n.-64-7075_-64-7074insACT
NM_000350.2:c.2744-71_2744-70insACT NP_000341.2:n.2744-71_2744-70insACT
NM_000350.3:c.2744-71_2744-70insACT MANE Select NP_000341.2:n.2744-71_2744-70insACT