Canonical Allele Identifier: CA2744619319
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94062847_94063052del , CM000663.2:g.94062847_94063052del GRCh38
NC_000001.10:g.94528403_94528608del , CM000663.1:g.94528403_94528608del GRCh37
NC_000001.9:g.94300991_94301196del NCBI36
NG_009073.1:g.63100_63305del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.1760+62_1761-92del MANE Select ENSP00000359245.3:n.1760+62_1761-92del
ENST00000649773.1:c.1760+62_1761-92del ENSP00000496882.1:n.1760+62_1761-92del
ENST00000370225.3:c.1760+62_1761-92del ENSP00000359245.3:n.1760+62_1761-92del
ENST00000536513.5:c.-65+124_-65+329del ENSP00000439707.2:n.-65+124_-65+329del
NM_000350.2:c.1760+62_1761-92del NP_000341.2:n.1760+62_1761-92del
NM_000350.3:c.1760+62_1761-92del MANE Select NP_000341.2:n.1760+62_1761-92del