Canonical Allele Identifier: CA2840573239
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94043279C>T , CM000663.2:g.94043279C>T GRCh38
NC_000001.10:g.94508835C>T , CM000663.1:g.94508835C>T GRCh37
NC_000001.9:g.94281423C>T NCBI36
NG_009073.1:g.82871G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.3190+57G>A MANE Select ENSP00000359245.3:n.3190+57G>A
ENST00000370225.3:c.3190+57G>A ENSP00000359245.3:n.3190+57G>A
ENST00000536513.5:c.-64-3190G>A ENSP00000439707.2:n.-64-3190G>A
NM_000350.2:c.3190+57G>A NP_000341.2:n.3190+57G>A
NM_000350.3:c.3190+57G>A MANE Select NP_000341.2:n.3190+57G>A