Canonical Allele Identifier: CA2744619279
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94062814_94062815insA , CM000663.2:g.94062814_94062815insA GRCh38
NC_000001.10:g.94528370_94528371insA , CM000663.1:g.94528370_94528371insA GRCh37
NC_000001.9:g.94300958_94300959insA NCBI36
NG_009073.1:g.63335_63336insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.1761-62_1761-61insT MANE Select ENSP00000359245.3:n.1761-62_1761-61insT
ENST00000649773.1:c.1761-62_1761-61insT ENSP00000496882.1:n.1761-62_1761-61insT
ENST00000370225.3:c.1761-62_1761-61insT ENSP00000359245.3:n.1761-62_1761-61insT
ENST00000536513.5:c.-65+359_-65+360insT ENSP00000439707.2:n.-65+359_-65+360insT
NM_000350.2:c.1761-62_1761-61insT NP_000341.2:n.1761-62_1761-61insT
NM_000350.3:c.1761-62_1761-61insT MANE Select NP_000341.2:n.1761-62_1761-61insT