Canonical Allele Identifier: CA2744619113
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94060808A>T , CM000663.2:g.94060808A>T GRCh38
NC_000001.10:g.94526364A>T , CM000663.1:g.94526364A>T GRCh37
NC_000001.9:g.94298952A>T NCBI36
NG_009073.1:g.65342T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.1938-49T>A MANE Select ENSP00000359245.3:n.1938-49T>A
ENST00000649773.1:c.1938-49T>A ENSP00000496882.1:n.1938-49T>A
ENST00000370225.3:c.1938-49T>A ENSP00000359245.3:n.1938-49T>A
ENST00000472033.1:n.58-49T>A
ENST00000536513.5:c.-65+2366T>A ENSP00000439707.2:n.-65+2366T>A
NM_000350.2:c.1938-49T>A NP_000341.2:n.1938-49T>A
NM_000350.3:c.1938-49T>A MANE Select NP_000341.2:n.1938-49T>A