Canonical Allele Identifier: CA645372217
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1152327
ClinVar RCV Id: RCV001493624
dbSNP Id: rs1659452688

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94008289_94008290delinsCA , CM000663.2:g.94008289_94008290delinsCA GRCh38
NC_000001.10:g.94473845_94473846delinsCA , CM000663.1:g.94473845_94473846delinsCA GRCh37
NC_000001.9:g.94246433_94246434delinsCA NCBI36
NG_009073.1:g.117860_117861delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.5843_5844delinsTG MANE Select ENSP00000359245.3:p.Pro1948Leu
ENST00000370225.3:c.5843_5844delinsTG ENSP00000359245.3:p.Pro1948Leu
ENST00000465352.1:n.259_260delinsTG
ENST00000536513.5:c.2219_2220delinsTG ENSP00000439707.2:p.Pro740Leu
NM_000350.2:c.5843_5844delinsTG NP_000341.2:p.Pro1948Leu
NM_000350.3:c.5843_5844delinsTG MANE Select NP_000341.2:p.Pro1948Leu